Linked Data
ClinVar Variation Id:
39021
dbSNP Id:
rs200646278
gnomAD v2:
12-102164207-G-A
gnomAD v3:
12-101770429-G-A
gnomAD v4:
12-101770429-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.101770429G>A , CM000674.2:g.101770429G>A | GRCh38 |
| NC_000012.11:g.102164207G>A , CM000674.1:g.102164207G>A | GRCh37 |
| NC_000012.10:g.100688338G>A | NCBI36 |
| NG_021243.1:g.65439C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000299314.12:c.1090C>T MANE Select | ENSP00000299314.7:p.Arg364Ter | |
| ENST00000299314.11:c.1090C>T | ENSP00000299314.7:p.Arg364Ter | |
| ENST00000549940.5:c.1090C>T | ENSP00000449150.1:p.Arg364Ter | |
| NM_024312.4:c.1090C>T | NP_077288.2:p.Arg364Ter | |
| XM_006719593.2:c.1090C>T | XP_006719656.1:p.Arg364Ter | |
| XM_011538731.1:c.1009C>T | XP_011537033.1:p.Arg337Ter | |
| XM_006719593.3:c.1090C>T | XP_006719656.1:p.Arg364Ter | |
| XM_011538731.2:c.1009C>T | XP_011537033.1:p.Arg337Ter | |
| XM_017019961.1:c.874C>T | XP_016875450.1:p.Arg292Ter | |
| XM_017019962.2:c.-138C>T | XP_016875451.1:n.-138C>T | |
| NM_024312.5:c.1090C>T MANE Select | NP_077288.2:p.Arg364Ter |