HGVS | Genome Assembly |
---|---|
NC_000002.12:g.188996170G= , CM000664.2:g.188996170G= | GRCh38 |
NC_000002.11:g.189860896G= , CM000664.1:g.189860896G= | GRCh37 |
NC_000002.10:g.189569141G= | NCBI36 |
NG_007404.1:g.26798G= , LRG_3:g.26798G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000450867.2:c.1555G= | ENSP00000415346.2:p.Gly519= | |
ENST00000304636.9:c.1654G= MANE Select | ENSP00000304408.4:p.Gly552= | |
ENST00000304636.7:c.1654G= | ENSP00000304408.3:p.Gly552= | |
ENST00000317840.9:c.1654G= | ENSP00000315243.6:p.Gly552= | |
NM_000090.3:c.1654G= , LRG_3t1:c.1654G= | NP_000081.1:p.Gly552= | |
NM_000090.4:c.1654G= MANE Select | NP_000081.2:p.Gly552= |