HGVS | Genome Assembly |
---|---|
NC_000001.11:g.154571200T= , CM000663.2:g.154571200T= | GRCh38 |
NC_000001.10:g.154543676T= , CM000663.1:g.154543676T= | GRCh37 |
NC_000001.9:g.152810300T= | NCBI36 |
NG_008027.1:g.8420T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000368476.4:c.377T= MANE Select | ENSP00000357461.3:p.Met126= | |
ENST00000636034.1:c.377T= | ENSP00000489703.1:p.Met126= | |
ENST00000637900.1:c.383T= | ENSP00000490474.1:p.Met128= | |
ENST00000368476.3:c.377T= | ENSP00000357461.3:p.Met126= | |
NM_000748.2:c.377T= | NP_000739.1:p.Met126= | |
XM_017000180.2:c.-9-125T= | XP_016855669.1:n.-9-125T= | |
XR_001736952.2:n.629T= | ||
NM_000748.3:c.377T= MANE Select | NP_000739.1:p.Met126= |