Linked Data
ClinVar Variation Id:
161356
dbSNP Id:
rs145924695
ExAC:
9:98220518 C / T
gnomAD v2:
9-98220518-C-T
gnomAD v3:
9-95458236-C-T
gnomAD v4:
9-95458236-C-T
PubMed:
PMID:23665959
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.95458236C>T , CM000671.2:g.95458236C>T | GRCh38 |
| NC_000009.11:g.98220518C>T , CM000671.1:g.98220518C>T | GRCh37 |
| NC_000009.10:g.97260339C>T | NCBI36 |
| NG_007664.1:g.63730G>A , LRG_515:g.63730G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000711046.1:c.2747G>A | ENSP00000518556.1:p.Arg916Gln | |
| ENST00000437951.6:c.2942G>A MANE Plus Clinical | ENSP00000389744.2:p.Arg981Gln | |
| ENST00000690194.1:c.*1253G>A | ENSP00000509379.1:n.*1253G>A | |
| ENST00000692981.1:c.2492G>A | ENSP00000510238.1:p.Arg831Gln | |
| ENST00000693534.1:n.276G>A | ||
| ENST00000331920.11:c.2945G>A MANE Select | ENSP00000332353.6:p.Arg982Gln | |
| ENST00000331920.10:c.2945G>A | ENSP00000332353.6:p.Arg982Gln | |
| ENST00000375274.6:c.2942G>A | ENSP00000364423.2:p.Arg981Gln | |
| ENST00000375290.6:c.2714G>A | ENSP00000364439.2:n.2714G>A | |
| ENST00000418258.5:c.2492G>A | ENSP00000396135.1:p.Arg831Gln | |
| ENST00000421141.5:c.2492G>A | ENSP00000399981.1:p.Arg831Gln | |
| ENST00000429896.6:c.2492G>A | ENSP00000414823.2:p.Arg831Gln | |
| ENST00000430669.6:c.2747G>A | ENSP00000410287.2:p.Arg916Gln | |
| ENST00000437951.5:c.2747G>A | ENSP00000389744.1:p.Arg916Gln | |
| ENST00000547615.1:n.295G>A | ||
| NM_000264.3:c.2945G>A , LRG_515t1:c.2945G>A | NP_000255.2:p.Arg982Gln | |
| NM_001083602.1:c.2747G>A , LRG_515t2:c.2747G>A | NP_001077071.1:p.Arg916Gln | |
| NM_001083603.1:c.2942G>A | NP_001077072.1:p.Arg981Gln | |
| NM_001083604.1:c.2492G>A | NP_001077073.1:p.Arg831Gln | |
| NM_001083605.1:c.2492G>A | NP_001077074.1:p.Arg831Gln | |
| NM_001083606.1:c.2492G>A | NP_001077075.1:p.Arg831Gln | |
| NM_001083607.1:c.2492G>A | NP_001077076.1:p.Arg831Gln | |
| XM_005252102.2:c.2492G>A | XP_005252159.1:p.Arg831Gln | |
| XM_011518868.1:c.2789G>A | XP_011517170.1:p.Arg930Gln | |
| XM_011518869.1:c.2492G>A | XP_011517171.1:p.Arg831Gln | |
| XM_011518870.1:c.2492G>A | XP_011517172.1:p.Arg831Gln | |
| XM_011518871.1:c.2492G>A | XP_011517173.1:p.Arg831Gln | |
| XM_011518872.1:c.2492G>A | XP_011517174.1:p.Arg831Gln | |
| XM_011518873.1:c.2105G>A | XP_011517175.1:p.Arg702Gln | |
| XM_011518874.1:c.2945G>A | XP_011517176.1:p.Arg982Gln | |
| NM_000264.4:c.2945G>A | NP_000255.2:p.Arg982Gln | |
| NM_001083602.2:c.2747G>A | NP_001077071.1:p.Arg916Gln | |
| NM_001083603.2:c.2942G>A | NP_001077072.1:p.Arg981Gln | |
| NM_001083604.2:c.2492G>A | NP_001077073.1:p.Arg831Gln | |
| NM_001083605.2:c.2492G>A | NP_001077074.1:p.Arg831Gln | |
| NM_001083606.2:c.2492G>A | NP_001077075.1:p.Arg831Gln | |
| NM_001083607.2:c.2492G>A | NP_001077076.1:p.Arg831Gln | |
| NM_001354918.1:c.2789G>A | NP_001341847.1:p.Arg930Gln | |
| NR_149061.1:n.2967G>A | ||
| NM_000264.5:c.2945G>A MANE Select | NP_000255.2:p.Arg982Gln | |
| NM_001083606.3:c.2492G>A | NP_001077075.1:p.Arg831Gln | |
| NM_001354918.2:c.2789G>A | NP_001341847.1:p.Arg930Gln | |
| NR_149061.2:n.3684G>A | ||
| NM_001083602.3:c.2747G>A | NP_001077071.1:p.Arg916Gln | |
| NM_001083603.3:c.2942G>A MANE Plus Clinical | NP_001077072.1:p.Arg981Gln | |
| NM_001083604.3:c.2492G>A | NP_001077073.1:p.Arg831Gln | |
| NM_001083605.3:c.2492G>A | NP_001077074.1:p.Arg831Gln | |
| NM_001083607.3:c.2492G>A | NP_001077076.1:p.Arg831Gln |