HGVS | Genome Assembly |
---|---|
NC_000001.11:g.156055308G= , CM000663.2:g.156055308G= | GRCh38 |
NC_000001.10:g.156025099G= , CM000663.1:g.156025099G= | GRCh37 |
NC_000001.9:g.154291723G= | NCBI36 |
NG_009898.1:g.5583G= , LRG_81:g.5583G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000368305.9:c.114G= MANE Select | ENSP00000357288.4:p.Gly38= | |
ENST00000368302.3:c.114G= | ENSP00000357285.3:p.Gly38= | |
ENST00000368304.9:c.114G= | ENSP00000357287.5:p.Gly38= | |
ENST00000368305.8:c.114G= | ENSP00000357288.4:p.Gly38= | |
ENST00000487106.5:n.224G= | ||
ENST00000489664.1:n.183G= | ||
NM_001145264.1:c.114G= | NP_001138736.1:p.Gly38= | |
NM_014017.3:c.114G= , LRG_81t1:c.114G= | NP_054736.1:p.Gly38= | |
NM_001145264.2:c.114G= | NP_001138736.1:p.Gly38= | |
NM_014017.4:c.114G= MANE Select | NP_054736.1:p.Gly38= |