HGVS | Genome Assembly |
---|---|
NC_000007.14:g.21749529T>A , CM000669.2:g.21749529T>A | GRCh38 |
NC_000007.13:g.21789147T>A , CM000669.1:g.21789147T>A | GRCh37 |
NC_000007.12:g.21755672T>A | NCBI36 |
NG_012886.2:g.211315T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000409508.8:c.8674-149T>A MANE Select | ENSP00000475939.1:n.8674-149T>A | |
ENST00000328843.10:c.8695-149T>A | ENSP00000330671.7:n.8695-149T>A | |
ENST00000409508.7:c.8674-149T>A | ENSP00000475939.1:n.8674-149T>A | |
ENST00000620169.4:c.8695-149T>A | ENSP00000481693.1:n.8695-149T>A | |
NM_001277115.1:c.8674-149T>A | NP_001264044.1:n.8674-149T>A | |
NM_001277115.2:c.8674-149T>A MANE Select | NP_001264044.1:n.8674-149T>A |