HGVS | Genome Assembly |
---|---|
NC_000006.12:g.18130688A= , CM000668.2:g.18130688A= | GRCh38 |
NC_000006.11:g.18130919A= , CM000668.1:g.18130919A= | GRCh37 |
NC_000006.10:g.18238898A= | NCBI36 |
NG_012137.2:g.29456T= | |
NG_012137.3:g.29456T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000309983.5:c.718T= MANE Select | ENSP00000312304.4:p.Tyr240= | |
ENST00000309983.4:c.718T= | ENSP00000312304.4:p.Tyr240= | |
NM_000367.3:c.718T= | NP_000358.1:p.Tyr240= | |
XM_011514839.1:c.673T= | XP_011513141.1:p.Tyr225= | |
XM_011514840.1:c.649T= | XP_011513142.1:p.Tyr217= | |
NM_000367.4:c.718T= | NP_000358.1:p.Tyr240= | |
NM_001346817.1:c.718T= | NP_001333746.1:p.Tyr240= | |
NM_001346818.1:c.673T= | NP_001333747.1:p.Tyr225= | |
NM_000367.5:c.718T= MANE Select | NP_000358.1:p.Tyr240= |