Canonical Allele Identifier: CA194717249
Gene: GNAQ HGNC NCBI

Linked Data

dbSNP Id: rs35942655
MyVariant Identifiers: chr9:g.80409307_80409308insC (hg19) chr9:g.77794391_77794392insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.77794394dup , CM000671.2:g.77794394dup GRCh38
NC_000009.11:g.80409310dup , CM000671.1:g.80409310dup GRCh37
NC_000009.10:g.79599130dup NCBI36
NG_027904.2:g.241912dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000286548.9:c.735+71dup MANE Select ENSP00000286548.4:n.735+71dup
ENST00000286548.8:c.735+71dup ENSP00000286548.4:n.735+71dup
NM_002072.4:c.735+71dup NP_002063.2:n.735+71dup
XM_017014628.2:c.561+71dup XP_016870117.1:n.561+71dup
NM_002072.5:c.735+71dup MANE Select NP_002063.2:n.735+71dup
Search 100 bp 5'
Search 100 bp 3'