Canonical Allele Identifier: CA1857429019

Gene: GNAQ

Linked Data

• dbSNP Id: rs1826620066

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.77794102_77794112del , CM000671.2:g.77794102_77794112del	GRCh38
NC_000009.11:g.80409018_80409028del , CM000671.1:g.80409018_80409028del	GRCh37
NC_000009.10:g.79598838_79598848del	NCBI36
NG_027904.2:g.242200_242210del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286548.9:c.735+359_735+369del MANE Select	ENSP00000286548.4:n.735+359_735+369del
ENST00000286548.8:c.735+359_735+369del	ENSP00000286548.4:n.735+359_735+369del
NM_002072.4:c.735+359_735+369del	NP_002063.2:n.735+359_735+369del
XM_017014628.2:c.561+359_561+369del	XP_016870117.1:n.561+359_561+369del
NM_002072.5:c.735+359_735+369del MANE Select	NP_002063.2:n.735+359_735+369del