Linked Data
ClinVar Variation Id:
2099193
ClinVar RCV Id:
RCV003021595
MyVariant Identifiers:
chr9:g.98244485C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.95482203C>T , CM000671.2:g.95482203C>T | GRCh38 |
| NC_000009.11:g.98244485C>T , CM000671.1:g.98244485C>T | GRCh37 |
| NC_000009.10:g.97284306C>T | NCBI36 |
| NG_007664.1:g.39763G>A , LRG_515:g.39763G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000711046.1:c.387G>A | ENSP00000518556.1:p.Arg129= | |
| ENST00000437951.6:c.582G>A MANE Plus Clinical | ENSP00000389744.2:p.Arg194= | |
| ENST00000690194.1:c.132G>A | ENSP00000509379.1:p.Arg44= | |
| ENST00000692981.1:c.132G>A | ENSP00000510238.1:p.Arg44= | |
| ENST00000331920.11:c.585G>A MANE Select | ENSP00000332353.6:p.Arg195= | |
| ENST00000331920.10:c.585G>A | ENSP00000332353.6:p.Arg195= | |
| ENST00000375274.6:c.582G>A | ENSP00000364423.2:p.Arg194= | |
| ENST00000375290.6:c.384-1615G>A | ENSP00000364439.2:n.384-1615G>A | |
| ENST00000418258.5:c.132G>A | ENSP00000396135.1:p.Arg44= | |
| ENST00000421141.5:c.132G>A | ENSP00000399981.1:p.Arg44= | |
| ENST00000429896.6:c.132G>A | ENSP00000414823.2:p.Arg44= | |
| ENST00000430669.6:c.387G>A | ENSP00000410287.2:p.Arg129= | |
| ENST00000437951.5:c.387G>A | ENSP00000389744.1:p.Arg129= | |
| ENST00000468211.6:c.387G>A | ENSP00000449745.1:p.Arg129= | |
| ENST00000546820.5:c.132G>A | ENSP00000448843.1:p.Arg44= | |
| ENST00000547672.5:c.132G>A | ENSP00000447878.1:p.Arg44= | |
| ENST00000548379.5:n.238G>A | ||
| ENST00000548420.1:c.-94-1615G>A | ENSP00000449078.1:n.-94-1615G>A | |
| ENST00000548945.6:n.194-1615G>A | ||
| ENST00000550136.1:n.2107G>A | ||
| ENST00000550914.6:c.167G>A | ENSP00000450047.1:p.Gly56Asp | |
| ENST00000551623.1:c.227G>A | ENSP00000447242.1:n.227G>A | |
| ENST00000551630.1:c.132G>A | ENSP00000450131.1:p.Arg44= | |
| ENST00000551845.5:c.132G>A | ENSP00000447008.1:p.Arg44= | |
| ENST00000553011.5:c.132G>A | ENSP00000447797.1:p.Arg44= | |
| ENST00000553256.5:n.331G>A | ||
| NM_000264.3:c.585G>A , LRG_515t1:c.585G>A | NP_000255.2:p.Arg195= | |
| NM_001083602.1:c.387G>A , LRG_515t2:c.387G>A | NP_001077071.1:p.Arg129= | |
| NM_001083603.1:c.582G>A | NP_001077072.1:p.Arg194= | |
| NM_001083604.1:c.132G>A | NP_001077073.1:p.Arg44= | |
| NM_001083605.1:c.132G>A | NP_001077074.1:p.Arg44= | |
| NM_001083606.1:c.132G>A | NP_001077075.1:p.Arg44= | |
| NM_001083607.1:c.132G>A | NP_001077076.1:p.Arg44= | |
| XM_005252102.2:c.132G>A | XP_005252159.1:p.Arg44= | |
| XM_011518868.1:c.585G>A | XP_011517170.1:p.Arg195= | |
| XM_011518869.1:c.132G>A | XP_011517171.1:p.Arg44= | |
| XM_011518870.1:c.132G>A | XP_011517172.1:p.Arg44= | |
| XM_011518871.1:c.132G>A | XP_011517173.1:p.Arg44= | |
| XM_011518872.1:c.132G>A | XP_011517174.1:p.Arg44= | |
| XM_011518873.1:c.-94-1615G>A | XP_011517175.1:n.-94-1615G>A | |
| XM_011518874.1:c.585G>A | XP_011517176.1:p.Arg195= | |
| NM_000264.4:c.585G>A | NP_000255.2:p.Arg195= | |
| NM_001083602.2:c.387G>A | NP_001077071.1:p.Arg129= | |
| NM_001083603.2:c.582G>A | NP_001077072.1:p.Arg194= | |
| NM_001083604.2:c.132G>A | NP_001077073.1:p.Arg44= | |
| NM_001083605.2:c.132G>A | NP_001077074.1:p.Arg44= | |
| NM_001083606.2:c.132G>A | NP_001077075.1:p.Arg44= | |
| NM_001083607.2:c.132G>A | NP_001077076.1:p.Arg44= | |
| NM_001354918.1:c.585G>A | NP_001341847.1:p.Arg195= | |
| NM_001354919.1:c.387G>A | NP_001341848.1:p.Arg129= | |
| NR_149061.1:n.773G>A | ||
| NM_000264.5:c.585G>A MANE Select | NP_000255.2:p.Arg195= | |
| NM_001083606.3:c.132G>A | NP_001077075.1:p.Arg44= | |
| NM_001354918.2:c.585G>A | NP_001341847.1:p.Arg195= | |
| NR_149061.2:n.1490G>A | ||
| NM_001083602.3:c.387G>A | NP_001077071.1:p.Arg129= | |
| NM_001083603.3:c.582G>A MANE Plus Clinical | NP_001077072.1:p.Arg194= | |
| NM_001083604.3:c.132G>A | NP_001077073.1:p.Arg44= | |
| NM_001083605.3:c.132G>A | NP_001077074.1:p.Arg44= | |
| NM_001083607.3:c.132G>A | NP_001077076.1:p.Arg44= | |
| NM_001354919.2:c.387G>A | NP_001341848.1:p.Arg129= |