Canonical Allele Identifier: CA10581328
Gene: GNAO1 HGNC NCBI

Linked Data

ClinVar Variation Id: 235488
ClinVar RCV Id: RCV000224477
dbSNP Id: rs878853051
MyVariant Identifiers: chr16:g.56388883A>G (hg19) chr16:g.56354971A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56354971A>G , CM000678.2:g.56354971A>G GRCh38
NC_000016.9:g.56388883A>G , CM000678.1:g.56388883A>G GRCh37
NC_000016.8:g.54946384A>G NCBI36
NG_042800.1:g.168633A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000262493.12:c.983A>G MANE Select ENSP00000262493.6:p.Asp328Gly
ENST00000562316.6:c.545-1132A>G ENSP00000457238.2:n.545-1132A>G
ENST00000564727.2:c.287A>G ENSP00000454971.2:p.Asp96Gly
ENST00000568375.2:c.221A>G
ENST00000638210.1:n.1283A>G
ENST00000638705.1:c.983A>G ENSP00000491223.1:p.Asp328Gly
ENST00000638836.1:n.893A>G
ENST00000639251.1:n.884A>G
ENST00000639268.1:c.618A>G
ENST00000639341.1:c.508A>G
ENST00000639770.1:c.1021A>G ENSP00000491999.1:n.1021A>G
ENST00000640390.1:n.913A>G
ENST00000640469.1:c.347A>G ENSP00000491875.1:p.Asp116Gly
ENST00000640560.1:n.759A>G
ENST00000640893.1:c.*381A>G ENSP00000492677.1:n.*381A>G
ENST00000262493.10:c.983A>G ENSP00000262493.6:p.Asp328Gly
ENST00000564727.1:c.203A>G ENSP00000454971.1:p.Asp68Gly
ENST00000568375.1:n.221A>G
NM_020988.2:c.983A>G NP_066268.1:p.Asp328Gly
XM_011523003.1:c.857A>G XP_011521305.1:p.Asp286Gly
XM_011523003.3:c.857A>G XP_011521305.1:p.Asp286Gly
NM_020988.3:c.983A>G MANE Select NP_066268.1:p.Asp328Gly
Search 100 bp 5'
Search 100 bp 3'