Canonical Allele Identifier: CA373997670
Gene: GNAQ HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.77794482A>C , CM000671.2:g.77794482A>C GRCh38
NC_000009.11:g.80409398A>C , CM000671.1:g.80409398A>C GRCh37
NC_000009.10:g.79599218A>C NCBI36
NG_027904.2:g.241822T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000286548.9:c.716T>G MANE Select ENSP00000286548.4:p.Leu239Arg
ENST00000286548.8:c.716T>G ENSP00000286548.4:p.Leu239Arg
NM_002072.4:c.716T>G NP_002063.2:p.Leu239Arg
XM_017014628.2:c.542T>G XP_016870117.1:p.Leu181Arg
NM_002072.5:c.716T>G MANE Select NP_002063.2:p.Leu239Arg