Canonical Allele Identifier: CA2580878312
Gene: GNAQ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.77794429A>C , CM000671.2:g.77794429A>C GRCh38
NC_000009.11:g.80409345A>C , CM000671.1:g.80409345A>C GRCh37
NC_000009.10:g.79599165A>C NCBI36
NG_027904.2:g.241875T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000286548.9:c.735+34T>G MANE Select ENSP00000286548.4:n.735+34T>G
ENST00000286548.8:c.735+34T>G ENSP00000286548.4:n.735+34T>G
NM_002072.4:c.735+34T>G NP_002063.2:n.735+34T>G
XM_017014628.2:c.561+34T>G XP_016870117.1:n.561+34T>G
NM_002072.5:c.735+34T>G MANE Select NP_002063.2:n.735+34T>G