Canonical Allele Identifier: CA1857429191
Gene: GNAQ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.77794318A= , CM000671.2:g.77794318A= GRCh38
NC_000009.11:g.80409234A= , CM000671.1:g.80409234A= GRCh37
NC_000009.10:g.79599054A= NCBI36
NG_027904.2:g.241986T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000286548.9:c.735+145T= MANE Select ENSP00000286548.4:n.735+145T=
ENST00000286548.8:c.735+145T= ENSP00000286548.4:n.735+145T=
NM_002072.4:c.735+145T= NP_002063.2:n.735+145T=
XM_017014628.2:c.561+145T= XP_016870117.1:n.561+145T=
NM_002072.5:c.735+145T= MANE Select NP_002063.2:n.735+145T=