Canonical Allele Identifier: CA281439755

Gene: GNAO1

Linked Data

• dbSNP Id: rs957130645
• gnomAD v3: 16-56351184-C-T
• gnomAD v4: 16-56351184-C-T
• MyVariant Identifiers: chr16:g.56385096C>T (hg19) ; chr16:g.56351184C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56351184C>T , CM000678.2:g.56351184C>T	GRCh38
NC_000016.9:g.56385096C>T , CM000678.1:g.56385096C>T	GRCh37
NC_000016.8:g.54942597C>T	NCBI36
NG_042800.1:g.164846C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000262493.12:c.724-200C>T MANE Select	ENSP00000262493.6:n.724-200C>T
ENST00000562316.6:c.391-200C>T	ENSP00000457238.2:n.391-200C>T
ENST00000564727.2:c.28-200C>T	ENSP00000454971.2:n.28-200C>T
ENST00000568375.2:c.116-3682C>T
ENST00000638185.1:n.939-200C>T
ENST00000638210.1:n.1024-200C>T
ENST00000638705.1:c.724-200C>T	ENSP00000491223.1:n.724-200C>T
ENST00000638836.1:n.634-200C>T
ENST00000639055.1:n.1445-200C>T
ENST00000639251.1:n.625-200C>T
ENST00000639268.1:c.359-200C>T
ENST00000639341.1:c.249-200C>T
ENST00000639770.1:c.762-200C>T	ENSP00000491999.1:n.762-200C>T
ENST00000640390.1:n.654-200C>T
ENST00000640469.1:c.88-200C>T	ENSP00000491875.1:n.88-200C>T
ENST00000640560.1:n.500-200C>T
ENST00000640893.1:c.*122-200C>T	ENSP00000492677.1:n.*122-200C>T
ENST00000262493.10:c.724-200C>T	ENSP00000262493.6:n.724-200C>T
ENST00000568375.1:n.116-3682C>T
NM_020988.2:c.724-200C>T	NP_066268.1:n.724-200C>T
XM_011523003.1:c.598-200C>T	XP_011521305.1:n.598-200C>T
XM_011523003.3:c.598-200C>T	XP_011521305.1:n.598-200C>T
NM_020988.3:c.724-200C>T MANE Select	NP_066268.1:n.724-200C>T