Canonical Allele Identifier: CA6429960

Gene: NANOG

Linked Data

• dbSNP Id: rs771687755
• ExAC: 12:7945627 C / T
• gnomAD v2: 12-7945627-C-T
• COSMIC: COSM4909739
• MyVariant Identifiers: chr12:g.7945627C>T (hg19) ; chr12:g.7793031C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.7793031C>T , CM000674.2:g.7793031C>T	GRCh38
NC_000012.11:g.7945627C>T , CM000674.1:g.7945627C>T	GRCh37
NC_000012.10:g.7836894C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229307.9:c.233C>T MANE Select	ENSP00000229307.4:p.Thr78Ile
ENST00000229307.8:c.233C>T	ENSP00000229307.4:p.Thr78Ile
ENST00000526286.1:c.233C>T	ENSP00000435288.1:p.Thr78Ile
ENST00000526434.2:n.377C>T
ENST00000541267.5:c.161C>T	ENSP00000444434.1:p.Thr54Ile
NM_001297698.1:c.233C>T	NP_001284627.1:p.Thr78Ile
NM_024865.3:c.233C>T	NP_079141.2:p.Thr78Ile
XM_011520850.1:c.233C>T	XP_011519152.1:p.Thr78Ile
XM_011520851.1:c.161C>T	XP_011519153.1:p.Thr54Ile
XM_011520852.1:c.-140C>T	XP_011519154.1:n.-140C>T
NM_024865.4:c.233C>T MANE Select	NP_079141.2:p.Thr78Ile
NM_001297698.2:c.233C>T	NP_001284627.1:p.Thr78Ile