Canonical Allele Identifier: CA944453049
Gene: NANOG HGNC NCBI

Linked Data

dbSNP Id: rs1862859390
gnomAD v3: 12-7792751-T-C
gnomAD v4: 12-7792751-T-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.7792751T>C , CM000674.2:g.7792751T>C GRCh38
NC_000012.11:g.7945347T>C , CM000674.1:g.7945347T>C GRCh37
NC_000012.10:g.7836614T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000229307.9:c.152-199T>C MANE Select ENSP00000229307.4:n.152-199T>C
ENST00000229307.8:c.152-199T>C ENSP00000229307.4:n.152-199T>C
ENST00000526286.1:c.152-199T>C ENSP00000435288.1:n.152-199T>C
ENST00000526434.2:n.334-237T>C
ENST00000541267.5:c.80-199T>C ENSP00000444434.1:n.80-199T>C
NM_001297698.1:c.152-199T>C NP_001284627.1:n.152-199T>C
NM_024865.3:c.152-199T>C NP_079141.2:n.152-199T>C
XM_011520850.1:c.152-199T>C XP_011519152.1:n.152-199T>C
XM_011520851.1:c.80-199T>C XP_011519153.1:n.80-199T>C
XM_011520852.1:c.-183-237T>C XP_011519154.1:n.-183-237T>C
NM_024865.4:c.152-199T>C MANE Select NP_079141.2:n.152-199T>C
NM_001297698.2:c.152-199T>C NP_001284627.1:n.152-199T>C
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