Canonical Allele Identifier: CA478527528

Gene: NANOG

Linked Data

• gnomAD v4: 12-7793035-T-G
• MyVariant Identifiers: chr12:g.7945631T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.7793035T>G , CM000674.2:g.7793035T>G	GRCh38
NC_000012.11:g.7945631T>G , CM000674.1:g.7945631T>G	GRCh37
NC_000012.10:g.7836898T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229307.9:c.237T>G MANE Select	ENSP00000229307.4:p.Ser79=
ENST00000229307.8:c.237T>G	ENSP00000229307.4:p.Ser79=
ENST00000526286.1:c.237T>G	ENSP00000435288.1:p.Ser79=
ENST00000526434.2:n.381T>G
ENST00000541267.5:c.165T>G	ENSP00000444434.1:p.Ser55=
NM_001297698.1:c.237T>G	NP_001284627.1:p.Ser79=
NM_024865.3:c.237T>G	NP_079141.2:p.Ser79=
XM_011520850.1:c.237T>G	XP_011519152.1:p.Ser79=
XM_011520851.1:c.165T>G	XP_011519153.1:p.Ser55=
XM_011520852.1:c.-136T>G	XP_011519154.1:n.-136T>G
NM_024865.4:c.237T>G MANE Select	NP_079141.2:p.Ser79=
NM_001297698.2:c.237T>G	NP_001284627.1:p.Ser79=