Canonical Allele Identifier: CA465578302
Gene: GNAQ HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.80409415A>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.77794499A>G , CM000671.2:g.77794499A>G GRCh38
NC_000009.11:g.80409415A>G , CM000671.1:g.80409415A>G GRCh37
NC_000009.10:g.79599235A>G NCBI36
NG_027904.2:g.241805T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000286548.9:c.699T>C MANE Select ENSP00000286548.4:p.Ser233=
ENST00000286548.8:c.699T>C ENSP00000286548.4:p.Ser233=
NM_002072.4:c.699T>C NP_002063.2:p.Ser233=
XM_017014628.2:c.525T>C XP_016870117.1:p.Ser175=
NM_002072.5:c.699T>C MANE Select NP_002063.2:p.Ser233=
Search 100 bp 5'
Search 100 bp 3'