HGVS | Genome Assembly |
---|---|
NC_000019.10:g.41424616T>A , CM000681.2:g.41424616T>A | GRCh38 |
NC_000019.9:g.41930521T>A , CM000681.1:g.41930521T>A | GRCh37 |
NC_000019.8:g.46622361T>A | NCBI36 |
NG_013004.1:g.31828T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000269980.7:c.*8T>A MANE Select | ENSP00000269980.2:n.*8T>A | |
ENST00000269980.6:c.*8T>A | ENSP00000269980.2:n.*8T>A | |
ENST00000457836.6:c.*8T>A | ENSP00000416000.2:n.*8T>A | |
ENST00000540732.3:c.*8T>A | ENSP00000443246.1:n.*8T>A | |
ENST00000544905.1:c.176T>A | ||
ENST00000595085.5:c.922+1919T>A | ENSP00000471150.2:n.922+1919T>A | |
NM_000709.3:c.*8T>A | NP_000700.1:n.*8T>A | |
NM_001164783.1:c.*8T>A | NP_001158255.1:n.*8T>A | |
NM_000709.4:c.*8T>A MANE Select | NP_000700.1:n.*8T>A | |
NM_001164783.2:c.*8T>A | NP_001158255.1:n.*8T>A |