HGVS | Genome Assembly |
---|---|
NC_000019.10:g.1401339C= , CM000681.2:g.1401339C= | GRCh38 |
NC_000019.9:g.1401338C= , CM000681.1:g.1401338C= | GRCh37 |
NC_000019.8:g.1352338C= | NCBI36 |
NG_009785.1:g.5215G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000252288.8:c.138G= MANE Select | ENSP00000252288.1:p.Glu46= | |
ENST00000447102.8:c.138G= | ENSP00000403536.2:p.Glu46= | |
ENST00000640762.1:c.112+26G= | ENSP00000492031.1:n.112+26G= | |
ENST00000252288.6:c.138G= | ENSP00000252288.1:p.Glu46= | |
ENST00000447102.7:c.138G= | ENSP00000403536.2:p.Glu46= | |
NM_000156.5:c.138G= | NP_000147.1:p.Glu46= | |
NM_138924.2:c.138G= | NP_620279.1:p.Glu46= | |
NM_000156.6:c.138G= MANE Select | NP_000147.1:p.Glu46= | |
NM_138924.3:c.138G= | NP_620279.1:p.Glu46= |