Canonical Allele Identifier: CA2719858859
Gene: GNAQ HGNC NCBI

Linked Data

dbSNP Id: rs2118444719

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.77794604A>C , CM000671.2:g.77794604A>C GRCh38
NC_000009.11:g.80409520A>C , CM000671.1:g.80409520A>C GRCh37
NC_000009.10:g.79599340A>C NCBI36
NG_027904.2:g.241700T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000286548.9:c.606-12T>G MANE Select ENSP00000286548.4:n.606-12T>G
ENST00000286548.8:c.606-12T>G ENSP00000286548.4:n.606-12T>G
NM_002072.4:c.606-12T>G NP_002063.2:n.606-12T>G
XM_017014628.2:c.432-12T>G XP_016870117.1:n.432-12T>G
NM_002072.5:c.606-12T>G MANE Select NP_002063.2:n.606-12T>G