HGVS | Genome Assembly |
---|---|
NC_000001.11:g.154571559G= , CM000663.2:g.154571559G= | GRCh38 |
NC_000001.10:g.154544035G= , CM000663.1:g.154544035G= | GRCh37 |
NC_000001.9:g.152810659G= | NCBI36 |
NG_008027.1:g.8779G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000368476.4:c.736G= MANE Select | ENSP00000357461.3:p.Val246= | |
ENST00000636034.1:c.736G= | ENSP00000489703.1:p.Val246= | |
ENST00000637900.1:c.742G= | ENSP00000490474.1:p.Val248= | |
ENST00000368476.3:c.736G= | ENSP00000357461.3:p.Val246= | |
NM_000748.2:c.736G= | NP_000739.1:p.Val246= | |
XM_017000180.2:c.226G= | XP_016855669.1:p.Val76= | |
XR_001736952.2:n.988G= | ||
NM_000748.3:c.736G= MANE Select | NP_000739.1:p.Val246= |