Linked Data
ClinVar Variation Id:
193923
dbSNP Id:
rs142756900
ExAC:
9:138651555 G / A
gnomAD v2:
9-138651555-G-A
gnomAD v3:
9-135759709-G-A
gnomAD v4:
9-135759709-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.135759709G>A , CM000671.2:g.135759709G>A | GRCh38 |
| NC_000009.11:g.138651555G>A , CM000671.1:g.138651555G>A | GRCh37 |
| NC_000009.10:g.137791376G>A | NCBI36 |
| NG_033070.1:g.62525G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000371757.7:c.885G>A MANE Select | ENSP00000360822.2:p.Ala295= | |
| ENST00000674572.1:c.726G>A | ENSP00000501742.1:p.Ala242= | |
| ENST00000675090.1:c.633G>A | ENSP00000501833.1:p.Ala211= | |
| ENST00000675399.1:c.633G>A | ENSP00000501932.1:p.Ala211= | |
| ENST00000676421.1:c.642G>A | ENSP00000502322.1:p.Ala214= | |
| ENST00000263604.5:c.786G>A | ENSP00000263604.4:p.Ala262= | |
| ENST00000371757.6:c.885G>A | ENSP00000360822.2:p.Ala295= | |
| ENST00000460750.5:c.*495G>A | ENSP00000418777.1:n.*495G>A | |
| ENST00000473941.5:c.726G>A | ENSP00000420764.1:p.Ala242= | |
| ENST00000486577.6:c.768G>A | ENSP00000417578.3:p.Ala256= | |
| ENST00000487664.5:c.885G>A | ENSP00000417851.2:p.Ala295= | |
| ENST00000488444.6:c.828G>A | ENSP00000419007.3:p.Ala276= | |
| ENST00000490355.6:c.828G>A | ENSP00000418003.3:p.Ala276= | |
| ENST00000490363.3:n.704G>A | ||
| ENST00000491806.6:c.828G>A | ENSP00000419086.3:p.Ala276= | |
| ENST00000628528.2:c.750G>A | ENSP00000486374.1:p.Ala250= | |
| ENST00000630792.2:c.726G>A | ENSP00000486486.1:p.Ala242= | |
| ENST00000631073.2:c.828G>A | ENSP00000486130.1:p.Ala276= | |
| NM_001272003.1:c.750G>A | NP_001258932.1:p.Ala250= | |
| NM_020822.2:c.885G>A | NP_065873.2:p.Ala295= | |
| XM_011518877.1:c.1020G>A | XP_011517179.1:p.Ala340= | |
| XM_011518878.1:c.1029G>A | XP_011517180.1:p.Ala343= | |
| XM_011518879.1:c.1020G>A | XP_011517181.1:p.Ala340= | |
| XM_011518880.1:c.786G>A | XP_011517182.1:p.Ala262= | |
| XM_011518881.1:c.375G>A | XP_011517183.1:p.Ala125= | |
| XM_011518877.3:c.1020G>A | XP_011517179.1:p.Ala340= | |
| XM_011518878.3:c.1029G>A | XP_011517180.1:p.Ala343= | |
| XM_011518879.3:c.1020G>A | XP_011517181.1:p.Ala340= | |
| XM_011518881.3:c.375G>A | XP_011517183.1:p.Ala125= | |
| XM_017014931.1:c.819G>A | XP_016870420.1:p.Ala273= | |
| XM_017014932.1:c.642G>A | XP_016870421.1:p.Ala214= | |
| XM_017014933.1:c.375G>A | XP_016870422.1:p.Ala125= | |
| XM_024447617.1:c.375G>A | XP_024303385.1:p.Ala125= | |
| XM_024447618.1:c.375G>A | XP_024303386.1:p.Ala125= | |
| NM_020822.3:c.885G>A MANE Select | NP_065873.2:p.Ala295= | |
| NM_001272003.2:c.750G>A | NP_001258932.1:p.Ala250= |