HGVS | Genome Assembly |
---|---|
NC_000017.11:g.58280398C= , CM000679.2:g.58280398C= | GRCh38 |
NC_000017.10:g.56357759C= , CM000679.1:g.56357759C= | GRCh37 |
NC_000017.9:g.53712758C= | NCBI36 |
NG_009629.1:g.5538G= , LRG_84:g.5538G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000225275.4:c.216G= MANE Select | ENSP00000225275.3:p.Leu72= | |
ENST00000225275.3:c.216G= | ENSP00000225275.3:p.Leu72= | |
ENST00000580005.1:n.145G= | ||
NM_000250.1:c.216G= , LRG_84t1:c.216G= | NP_000241.1:p.Leu72= | |
XM_011524821.1:c.402G= | XP_011523123.1:p.Leu134= | |
XM_011524822.1:c.-38+207G= | XP_011523124.1:n.-38+207G= | |
XM_011524823.1:c.402G= | XP_011523125.1:p.Leu134= | |
NM_000250.2:c.216G= MANE Select | NP_000241.1:p.Leu72= |