HGVS | Genome Assembly |
---|---|
NC_000007.14:g.95324608A>C , CM000669.2:g.95324608A>C | GRCh38 |
NC_000007.13:g.94953920A>C , CM000669.1:g.94953920A>C | GRCh37 |
NC_000007.12:g.94791856A>C | NCBI36 |
NG_008779.1:g.4965T>G | |
NG_008779.2:g.5099T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000222381.7:c.-133T>G | ENSP00000222381.3:n.-133T>G | |
NM_000446.6:c.-133T>G | NP_000437.3:n.-133T>G |