Canonical Allele Identifier: CA2719613905
Gene: GNAQ HGNC NCBI

Linked Data

dbSNP Id: rs1188478402
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.77794444C>G , CM000671.2:g.77794444C>G GRCh38
NC_000009.11:g.80409360C>G , CM000671.1:g.80409360C>G GRCh37
NC_000009.10:g.79599180C>G NCBI36
NG_027904.2:g.241860G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000286548.9:c.735+19G>C MANE Select ENSP00000286548.4:n.735+19G>C
ENST00000286548.8:c.735+19G>C ENSP00000286548.4:n.735+19G>C
NM_002072.4:c.735+19G>C NP_002063.2:n.735+19G>C
XM_017014628.2:c.561+19G>C XP_016870117.1:n.561+19G>C
NM_002072.5:c.735+19G>C MANE Select NP_002063.2:n.735+19G>C
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