Linked Data
dbSNP Id:
rs767494902
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.53560624G>T , CM000667.2:g.53560624G>T | GRCh38 |
| NC_000005.9:g.52856454G>T , CM000667.1:g.52856454G>T | GRCh37 |
| NC_000005.8:g.52892211G>T | NCBI36 |
| NG_008200.1:g.4990G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011543414.1:c.-39G>T | XP_011541716.1:n.-39G>T | |
| XM_017009491.1:c.-39G>T | XP_016864980.1:n.-39G>T |