Canonical Allele Identifier: CA373997668
Gene: GNAQ HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000286548.9:c.716T>C MANE Select ENSP00000286548.4:p.Leu239Pro
ENST00000286548.8:c.716T>C ENSP00000286548.4:p.Leu239Pro
NM_002072.4:c.716T>C NP_002063.2:p.Leu239Pro
XM_017014628.2:c.542T>C XP_016870117.1:p.Leu181Pro
NM_002072.5:c.716T>C MANE Select NP_002063.2:p.Leu239Pro