Canonical Allele Identifier: CA1857429051
Gene: GNAQ HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.77794148T= , CM000671.2:g.77794148T= GRCh38
NC_000009.11:g.80409064T= , CM000671.1:g.80409064T= GRCh37
NC_000009.10:g.79598884T= NCBI36
NG_027904.2:g.242156A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000286548.9:c.735+315A= MANE Select ENSP00000286548.4:n.735+315A=
ENST00000286548.8:c.735+315A= ENSP00000286548.4:n.735+315A=
NM_002072.4:c.735+315A= NP_002063.2:n.735+315A=
XM_017014628.2:c.561+315A= XP_016870117.1:n.561+315A=
NM_002072.5:c.735+315A= MANE Select NP_002063.2:n.735+315A=
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