Canonical Allele Identifier: CA2719587926
Gene: GNAQ HGNC NCBI

Linked Data

dbSNP Id: rs372136969
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.77794454A>T , CM000671.2:g.77794454A>T GRCh38
NC_000009.11:g.80409370A>T , CM000671.1:g.80409370A>T GRCh37
NC_000009.10:g.79599190A>T NCBI36
NG_027904.2:g.241850T>A

Transcript Alleles

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