HGVS | Genome Assembly |
---|---|
NC_000020.11:g.31820150G= , CM000682.2:g.31820150G= | GRCh38 |
NC_000020.10:g.30407953G= , CM000682.1:g.30407953G= | GRCh37 |
NC_000020.9:g.29871614G= | NCBI36 |
NG_012847.1:g.5776G= , LRG_392:g.5776G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375985.5:c.77G= MANE Select | ENSP00000365152.4:p.Gly26= | |
ENST00000375985.4:c.77G= | ENSP00000365152.4:p.Gly26= | |
ENST00000375994.6:c.77G= | ENSP00000365162.2:p.Gly26= | |
NM_033118.3:c.77G= , LRG_392t1:c.77G= | NP_149109.1:p.Gly26= | |
XR_244155.1:n.242G= | ||
NM_033118.4:c.77G= MANE Select | NP_149109.1:p.Gly26= |