HGVS | Genome Assembly |
---|---|
NC_000007.14:g.21705353G>A , CM000669.2:g.21705353G>A | GRCh38 |
NC_000007.13:g.21744971G>A , CM000669.1:g.21744971G>A | GRCh37 |
NC_000007.12:g.21711496G>A | NCBI36 |
NG_012886.2:g.167139G>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000409508.8:c.6469-107G>A MANE Select | ENSP00000475939.1:n.6469-107G>A | |
ENST00000328843.10:c.6490-107G>A | ENSP00000330671.7:n.6490-107G>A | |
ENST00000409508.7:c.6469-107G>A | ENSP00000475939.1:n.6469-107G>A | |
ENST00000620169.4:c.6490-107G>A | ENSP00000481693.1:n.6490-107G>A | |
NM_001277115.1:c.6469-107G>A | NP_001264044.1:n.6469-107G>A | |
NM_001277115.2:c.6469-107G>A MANE Select | NP_001264044.1:n.6469-107G>A |