Linked Data
ClinVar Variation Id:
454521
dbSNP Id:
rs1034327724
gnomAD v2:
6-116949323-C-T
gnomAD v3:
6-116628160-C-T
gnomAD v4:
6-116628160-C-T
COSMIC:
COSM1072432
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.116628160C>T , CM000668.2:g.116628160C>T | GRCh38 |
| NC_000006.11:g.116949323C>T , CM000668.1:g.116949323C>T | GRCh37 |
| NC_000006.10:g.117056016C>T | NCBI36 |
| NG_012934.1:g.16682C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000229554.10:c.1453C>T MANE Select | ENSP00000229554.5:p.Arg485Ter | |
| ENST00000229554.9:c.1453C>T | ENSP00000229554.5:p.Arg485Ter | |
| ENST00000368580.4:c.922-1407C>T | ENSP00000357569.4:n.922-1407C>T | |
| ENST00000368581.8:c.1453C>T | ENSP00000357570.4:p.Arg485Ter | |
| NM_001010892.2:c.1453C>T | NP_001010892.1:p.Arg485Ter | |
| NM_001161664.1:c.1453C>T | NP_001155136.1:p.Arg485Ter | |
| XM_006715469.2:c.1453C>T | XP_006715532.1:p.Arg485Ter | |
| XM_011535791.1:c.1453C>T | XP_011534093.1:p.Arg485Ter | |
| XM_011535792.1:c.1453C>T | XP_011534094.1:p.Arg485Ter | |
| XR_942416.1:n.4104C>T | ||
| XM_017010826.1:c.1453C>T | XP_016866315.1:p.Arg485Ter | |
| NM_001010892.3:c.1453C>T MANE Select | NP_001010892.1:p.Arg485Ter | |
| NM_001161664.2:c.1453C>T | NP_001155136.1:p.Arg485Ter |