Canonical Allele Identifier: CA373997652
Gene: GNAQ HGNC NCBI

Linked Data

dbSNP Id: rs2118442874

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.77794474A>C , CM000671.2:g.77794474A>C GRCh38
NC_000009.11:g.80409390A>C , CM000671.1:g.80409390A>C GRCh37
NC_000009.10:g.79599210A>C NCBI36
NG_027904.2:g.241830T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000286548.9:c.724T>G MANE Select ENSP00000286548.4:p.Ser242Ala
ENST00000286548.8:c.724T>G ENSP00000286548.4:p.Ser242Ala
NM_002072.4:c.724T>G NP_002063.2:p.Ser242Ala
XM_017014628.2:c.550T>G XP_016870117.1:p.Ser184Ala
NM_002072.5:c.724T>G MANE Select NP_002063.2:p.Ser242Ala