Canonical Allele Identifier: CA867169091
Gene: GNAQ HGNC NCBI

Linked Data

dbSNP Id: rs1352789080
MyVariant Identifiers: chr9:g.80409214G>A (hg19) chr9:g.77794298G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.77794298G>A , CM000671.2:g.77794298G>A GRCh38
NC_000009.11:g.80409214G>A , CM000671.1:g.80409214G>A GRCh37
NC_000009.10:g.79599034G>A NCBI36
NG_027904.2:g.242006C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000286548.9:c.735+165C>T MANE Select ENSP00000286548.4:n.735+165C>T
ENST00000286548.8:c.735+165C>T ENSP00000286548.4:n.735+165C>T
NM_002072.4:c.735+165C>T NP_002063.2:n.735+165C>T
XM_017014628.2:c.561+165C>T XP_016870117.1:n.561+165C>T
NM_002072.5:c.735+165C>T MANE Select NP_002063.2:n.735+165C>T
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