Linked Data
ClinVar Variation Id:
96439
dbSNP Id:
rs398124500
gnomAD v2:
6-51618125-G-A
gnomAD v3:
6-51753327-G-A
gnomAD v4:
6-51753327-G-A
COSMIC:
COSM220247
PubMed:
PMID:19940839
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.51753327G>A , CM000668.2:g.51753327G>A | GRCh38 |
| NC_000006.11:g.51618125G>A , CM000668.1:g.51618125G>A | GRCh37 |
| NC_000006.10:g.51726084G>A | NCBI36 |
| NG_008753.1:g.339299C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371117.8:c.8824C>T MANE Select | ENSP00000360158.3:p.Arg2942Ter | |
| ENST00000340994.4:c.8824C>T | ENSP00000341097.4:p.Arg2942Ter | |
| ENST00000371117.7:c.8824C>T | ENSP00000360158.3:p.Arg2942Ter | |
| NM_138694.3:c.8824C>T | NP_619639.3:p.Arg2942Ter | |
| NM_170724.2:c.8824C>T | NP_733842.2:p.Arg2942Ter | |
| XM_011514679.1:c.8824C>T | XP_011512981.1:p.Arg2942Ter | |
| XM_011514680.1:c.8824C>T | XP_011512982.1:p.Arg2942Ter | |
| XM_011514681.1:c.8695C>T | XP_011512983.1:p.Arg2899Ter | |
| XM_011514682.1:c.8686C>T | XP_011512984.1:p.Arg2896Ter | |
| XM_011514683.1:c.8182C>T | XP_011512985.1:p.Arg2728Ter | |
| XM_011514684.1:c.8113C>T | XP_011512986.1:p.Arg2705Ter | |
| XM_011514685.1:c.8824C>T | XP_011512987.1:p.Arg2942Ter | |
| XM_011514686.1:c.8824C>T | XP_011512988.1:p.Arg2942Ter | |
| XM_011514687.1:c.8824C>T | XP_011512989.1:p.Arg2942Ter | |
| XM_011514688.1:c.8824C>T | XP_011512990.1:p.Arg2942Ter | |
| XM_011514690.1:c.2899C>T | XP_011512992.1:p.Arg967Ter | |
| XM_011514691.1:c.2899C>T | XP_011512993.1:p.Arg967Ter | |
| XM_011514680.3:c.8824C>T | XP_011512982.1:p.Arg2942Ter | |
| XM_011514682.3:c.8686C>T | XP_011512984.1:p.Arg2896Ter | |
| XM_011514683.3:c.8182C>T | XP_011512985.1:p.Arg2728Ter | |
| XM_011514684.3:c.8113C>T | XP_011512986.1:p.Arg2705Ter | |
| XM_011514686.2:c.8824C>T | XP_011512988.1:p.Arg2942Ter | |
| XM_011514688.2:c.8824C>T | XP_011512990.1:p.Arg2942Ter | |
| XM_011514690.3:c.2899C>T | XP_011512992.1:p.Arg967Ter | |
| XM_011514691.3:c.2899C>T | XP_011512993.1:p.Arg967Ter | |
| XM_017010944.2:c.8824C>T | XP_016866433.1:p.Arg2942Ter | |
| XM_017010945.2:c.8749C>T | XP_016866434.1:p.Arg2917Ter | |
| XM_017010946.2:c.8629C>T | XP_016866435.1:p.Arg2877Ter | |
| XM_017010947.2:c.8560C>T | XP_016866436.1:p.Arg2854Ter | |
| XM_017010948.2:c.8113C>T | XP_016866437.1:p.Arg2705Ter | |
| XM_017010949.2:c.6964C>T | XP_016866438.1:p.Arg2322Ter | |
| XM_017010950.1:c.8824C>T | XP_016866439.1:p.Arg2942Ter | |
| XM_017010951.1:c.*1428C>T | XP_016866440.1:n.*1428C>T | |
| XR_001743469.1:n.9100C>T | ||
| NM_138694.4:c.8824C>T MANE Select | NP_619639.3:p.Arg2942Ter | |
| NM_170724.3:c.8824C>T | NP_733842.2:p.Arg2942Ter |