Canonical Allele Identifier: CA1857429260
Gene: GNAQ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.77794393C= , CM000671.2:g.77794393C= GRCh38
NC_000009.11:g.80409309C= , CM000671.1:g.80409309C= GRCh37
NC_000009.10:g.79599129C= NCBI36
NG_027904.2:g.241911G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000286548.9:c.735+70G= MANE Select ENSP00000286548.4:n.735+70G=
ENST00000286548.8:c.735+70G= ENSP00000286548.4:n.735+70G=
NM_002072.4:c.735+70G= NP_002063.2:n.735+70G=
XM_017014628.2:c.561+70G= XP_016870117.1:n.561+70G=
NM_002072.5:c.735+70G= MANE Select NP_002063.2:n.735+70G=