HGVS | Genome Assembly |
---|---|
NC_000012.12:g.6044348A= , CM000674.2:g.6044348A= | GRCh38 |
NC_000012.11:g.6153514A= , CM000674.1:g.6153514A= | GRCh37 |
NC_000012.10:g.6023775A= | NCBI36 |
NG_009072.1:g.85323T= | |
NG_009072.2:g.85323T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000261405.10:c.2385T= MANE Select | ENSP00000261405.5:p.Tyr795= | |
ENST00000261405.9:c.2385T= | ENSP00000261405.5:p.Tyr795= | |
ENST00000538635.5:n.421-50414T= | ||
NM_000552.3:c.2385T= | NP_000543.2:p.Tyr795= | |
NM_000552.4:c.2385T= | NP_000543.2:p.Tyr795= | |
NM_000552.5:c.2385T= MANE Select | NP_000543.3:p.Tyr795= |