Linked Data
dbSNP Id:
rs10787760
gnomAD v2:
10-118890693-G-A
gnomAD v3:
10-117131182-G-A
gnomAD v4:
10-117131182-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.117131182G>A , CM000672.2:g.117131182G>A | GRCh38 |
| NC_000010.10:g.118890693G>A , CM000672.1:g.118890693G>A | GRCh37 |
| NC_000010.9:g.118880683G>A | NCBI36 |
| NG_012317.1:g.12120C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000277905.6:c.*1027C>T | ENSP00000277905.2:n.*1027C>T | |
| NM_199131.2:c.*1027C>T | NP_954582.1:n.*1027C>T | |
| NM_199131.3:c.*1027C>T | NP_954582.1:n.*1027C>T |