Canonical Allele Identifier: CA721963738

Gene: GNAO1

Linked Data

• dbSNP Id: rs1454901506
• gnomAD v3: 16-56354802-C-G
• gnomAD v4: 16-56354802-C-G
• MyVariant Identifiers: chr16:g.56388714C>G (hg19) ; chr16:g.56354802C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56354802C>G , CM000678.2:g.56354802C>G	GRCh38
NC_000016.9:g.56388714C>G , CM000678.1:g.56388714C>G	GRCh37
NC_000016.8:g.54946215C>G	NCBI36
NG_042800.1:g.168464C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262493.12:c.878-64C>G MANE Select	ENSP00000262493.6:n.878-64C>G
ENST00000562316.6:c.545-1301C>G	ENSP00000457238.2:n.545-1301C>G
ENST00000564727.2:c.182-64C>G	ENSP00000454971.2:n.182-64C>G
ENST00000568375.2:c.116-64C>G
ENST00000638185.1:n.1093-64C>G
ENST00000638210.1:n.1178-64C>G
ENST00000638705.1:c.878-64C>G	ENSP00000491223.1:n.878-64C>G
ENST00000638836.1:n.788-64C>G
ENST00000639055.1:n.1599-64C>G
ENST00000639251.1:n.779-64C>G
ENST00000639268.1:c.513-64C>G
ENST00000639341.1:c.403-64C>G
ENST00000639770.1:c.916-64C>G	ENSP00000491999.1:n.916-64C>G
ENST00000640390.1:n.808-64C>G
ENST00000640469.1:c.242-64C>G	ENSP00000491875.1:n.242-64C>G
ENST00000640560.1:n.654-64C>G
ENST00000640893.1:c.*276-64C>G	ENSP00000492677.1:n.*276-64C>G
ENST00000262493.10:c.878-64C>G	ENSP00000262493.6:n.878-64C>G
ENST00000564727.1:c.98-64C>G	ENSP00000454971.1:n.98-64C>G
ENST00000568375.1:n.116-64C>G
NM_020988.2:c.878-64C>G	NP_066268.1:n.878-64C>G
XM_011523003.1:c.752-64C>G	XP_011521305.1:n.752-64C>G
XM_011523003.3:c.752-64C>G	XP_011521305.1:n.752-64C>G
NM_020988.3:c.878-64C>G MANE Select	NP_066268.1:n.878-64C>G