HGVS | Genome Assembly |
---|---|
NC_000012.12:g.52520369A>T , CM000674.2:g.52520369A>T | GRCh38 |
NC_000012.11:g.52914153A>T , CM000674.1:g.52914153A>T | GRCh37 |
NC_000012.10:g.51200420A>T | NCBI36 |
NG_008297.1:g.5091T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000252242.9:c.-73T>A MANE Select | ENSP00000252242.4:n.-73T>A | |
ENST00000252242.8:c.-73T>A | ENSP00000252242.4:n.-73T>A | |
ENST00000546577.1:c.-13+28T>A | ENSP00000449651.1:n.-13+28T>A | |
ENST00000549420.1:c.-73T>A | ENSP00000447209.1:n.-73T>A | |
ENST00000551275.1:c.-73T>A | ENSP00000448041.1:n.-73T>A | |
ENST00000552629.5:n.26T>A | ||
NM_000424.3:c.-73T>A | NP_000415.2:n.-73T>A | |
NM_000424.4:c.-73T>A MANE Select | NP_000415.2:n.-73T>A |