Canonical Allele Identifier: CA1857429097
Gene: GNAQ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.77794205T= , CM000671.2:g.77794205T= GRCh38
NC_000009.11:g.80409121T= , CM000671.1:g.80409121T= GRCh37
NC_000009.10:g.79598941T= NCBI36
NG_027904.2:g.242099A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000286548.9:c.735+258A= MANE Select ENSP00000286548.4:n.735+258A=
ENST00000286548.8:c.735+258A= ENSP00000286548.4:n.735+258A=
NM_002072.4:c.735+258A= NP_002063.2:n.735+258A=
XM_017014628.2:c.561+258A= XP_016870117.1:n.561+258A=
NM_002072.5:c.735+258A= MANE Select NP_002063.2:n.735+258A=