Canonical Allele Identifier: CA1857429381
Gene: GNAQ HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.77794493A= , CM000671.2:g.77794493A= GRCh38
NC_000009.11:g.80409409A= , CM000671.1:g.80409409A= GRCh37
NC_000009.10:g.79599229A= NCBI36
NG_027904.2:g.241811T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000286548.9:c.705T= MANE Select ENSP00000286548.4:p.Tyr235=
ENST00000286548.8:c.705T= ENSP00000286548.4:p.Tyr235=
NM_002072.4:c.705T= NP_002063.2:p.Tyr235=
XM_017014628.2:c.531T= XP_016870117.1:p.Tyr177=
NM_002072.5:c.705T= MANE Select NP_002063.2:p.Tyr235=
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