HGVS | Genome Assembly |
---|---|
NC_000001.11:g.12746532G>A , CM000663.2:g.12746532G>A | GRCh38 |
NC_000001.10:g.12806480G>A , CM000663.1:g.12806480G>A | GRCh37 |
NC_000001.9:g.12729067G>A | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000614859.5:c.102G>A MANE Select | ENSP00000477802.1:p.Glu34= | |
ENST00000376210.3:c.102G>A | ENSP00000365383.3:p.Glu34= | |
ENST00000474179.1:n.146G>A | ||
ENST00000614859.4:c.102G>A | ENSP00000477802.1:p.Glu34= | |
NM_152290.3:c.102G>A | NP_689503.3:p.Glu34= | |
XM_011542434.1:c.102G>A | XP_011540736.1:p.Glu34= | |
NM_001330361.1:c.102G>A | NP_001317290.1:p.Glu34= | |
NM_152290.4:c.102G>A MANE Select | NP_689503.3:p.Glu34= | |
NM_001330361.2:c.102G>A | NP_001317290.1:p.Glu34= |