HGVS | Genome Assembly |
---|---|
NC_000009.12:g.101421742A>T , CM000671.2:g.101421742A>T | GRCh38 |
NC_000009.11:g.104184024A>T , CM000671.1:g.104184024A>T | GRCh37 |
NC_000009.10:g.103223845A>T | NCBI36 |
NG_012387.1:g.19039T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000647789.2:c.*67T>A MANE Select | ENSP00000497767.1:n.*67T>A | |
ENST00000648064.1:c.*67T>A | ENSP00000497990.1:n.*67T>A | |
ENST00000648758.1:c.*67T>A | ENSP00000497731.1:n.*67T>A | |
ENST00000374855.8:c.*67T>A | ENSP00000363988.4:n.*67T>A | |
ENST00000616752.1:c.*174T>A | ENSP00000481363.1:n.*174T>A | |
NM_000035.3:c.*67T>A | NP_000026.2:n.*67T>A | |
NM_000035.4:c.*67T>A MANE Select | NP_000026.2:n.*67T>A |