HGVS | Genome Assembly |
---|---|
NC_000012.12:g.91111692T>G , CM000674.2:g.91111692T>G | GRCh38 |
NC_000012.11:g.91505469T>G , CM000674.1:g.91505469T>G | GRCh37 |
NC_000012.10:g.90029600T>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000266718.4:c.-316A>C | ENSP00000266718.4:n.-316A>C | |
NM_002345.3:c.-316A>C | NP_002336.1:n.-316A>C |