Canonical Allele Identifier: CA383780301

Gene: NANOG

Linked Data

• dbSNP Id: rs1862863416
• gnomAD v4: 12-7793025-A-G
• MyVariant Identifiers: chr12:g.7945621A>G (hg19) ; chr12:g.7793025A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.7793025A>G , CM000674.2:g.7793025A>G	GRCh38
NC_000012.11:g.7945621A>G , CM000674.1:g.7945621A>G	GRCh37
NC_000012.10:g.7836888A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229307.9:c.227A>G MANE Select	ENSP00000229307.4:p.Gln76Arg
ENST00000229307.8:c.227A>G	ENSP00000229307.4:p.Gln76Arg
ENST00000526286.1:c.227A>G	ENSP00000435288.1:p.Gln76Arg
ENST00000526434.2:n.371A>G
ENST00000541267.5:c.155A>G	ENSP00000444434.1:p.Gln52Arg
NM_001297698.1:c.227A>G	NP_001284627.1:p.Gln76Arg
NM_024865.3:c.227A>G	NP_079141.2:p.Gln76Arg
XM_011520850.1:c.227A>G	XP_011519152.1:p.Gln76Arg
XM_011520851.1:c.155A>G	XP_011519153.1:p.Gln52Arg
XM_011520852.1:c.-146A>G	XP_011519154.1:n.-146A>G
NM_024865.4:c.227A>G MANE Select	NP_079141.2:p.Gln76Arg
NM_001297698.2:c.227A>G	NP_001284627.1:p.Gln76Arg