Canonical Allele Identifier: CA232550169

Gene: NANOG

Linked Data

• dbSNP Id: rs758002314
• gnomAD v4: 12-7793217-G-C
• MyVariant Identifiers: chr12:g.7945813G>C (hg19) ; chr12:g.7793217G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.7793217G>C , CM000674.2:g.7793217G>C	GRCh38
NC_000012.11:g.7945813G>C , CM000674.1:g.7945813G>C	GRCh37
NC_000012.10:g.7837080G>C	NCBI36

Transcript Alleles

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