Canonical Allele Identifier: CA6429994

Gene: NANOG

Linked Data

• dbSNP Id: rs765153457
• ExAC: 12:7945814 C / A
• gnomAD v2: 12-7945814-C-A
• gnomAD v4: 12-7793218-C-A
• MyVariant Identifiers: chr12:g.7945814C>A (hg19) ; chr12:g.7793218C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.7793218C>A , CM000674.2:g.7793218C>A	GRCh38
NC_000012.11:g.7945814C>A , CM000674.1:g.7945814C>A	GRCh37
NC_000012.10:g.7837081C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229307.9:c.414+6C>A MANE Select	ENSP00000229307.4:n.414+6C>A
ENST00000229307.8:c.414+6C>A	ENSP00000229307.4:n.414+6C>A
ENST00000526286.1:c.414+6C>A	ENSP00000435288.1:n.414+6C>A
ENST00000541267.5:c.342+6C>A	ENSP00000444434.1:n.342+6C>A
NM_001297698.1:c.414+6C>A	NP_001284627.1:n.414+6C>A
NM_024865.3:c.414+6C>A	NP_079141.2:n.414+6C>A
XM_011520850.1:c.414+6C>A	XP_011519152.1:n.414+6C>A
XM_011520851.1:c.342+6C>A	XP_011519153.1:n.342+6C>A
XM_011520852.1:c.42+6C>A	XP_011519154.1:n.42+6C>A
NM_024865.4:c.414+6C>A MANE Select	NP_079141.2:n.414+6C>A
NM_001297698.2:c.414+6C>A	NP_001284627.1:n.414+6C>A