Linked Data
dbSNP Id:
rs1450328907
gnomAD v2:
10-115804131-C-T
gnomAD v3:
10-114044372-C-T
gnomAD v4:
10-114044372-C-T
COSMIC:
COSM4480326
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.114044372C>T , CM000672.2:g.114044372C>T | GRCh38 |
| NC_000010.10:g.115804131C>T , CM000672.1:g.115804131C>T | GRCh37 |
| NC_000010.9:g.115794121C>T | NCBI36 |
| NG_012187.1:g.5326C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369295.4:c.240C>T MANE Select | ENSP00000358301.2:p.Ile80= | |
| ENST00000369295.3:c.240C>T | ENSP00000358301.2:p.Ile80= | |
| NM_000684.2:c.240C>T | NP_000675.1:p.Ile80= | |
| NM_000684.3:c.240C>T MANE Select | NP_000675.1:p.Ile80= |