HGVS | Genome Assembly |
---|---|
NC_000012.12:g.6023770A>T , CM000674.2:g.6023770A>T | GRCh38 |
NC_000012.11:g.6132936A>T , CM000674.1:g.6132936A>T | GRCh37 |
NC_000012.10:g.6003197A>T | NCBI36 |
NG_009072.1:g.105901T>A | |
NG_009072.2:g.105901T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261405.10:c.3240T>A MANE Select | ENSP00000261405.5:p.Tyr1080Ter | |
ENST00000261405.9:c.3240T>A | ENSP00000261405.5:p.Tyr1080Ter | |
ENST00000538635.5:n.421-29836T>A | ||
NM_000552.3:c.3240T>A | NP_000543.2:p.Tyr1080Ter | |
NM_000552.4:c.3240T>A | NP_000543.2:p.Tyr1080Ter | |
NM_000552.5:c.3240T>A MANE Select | NP_000543.3:p.Tyr1080Ter |