Canonical Allele Identifier: CA6429974
Gene: NANOG HGNC NCBI

Linked Data

dbSNP Id: rs777708163
gnomAD v2: 12-7945661-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.7793065C>G , CM000674.2:g.7793065C>G GRCh38
NC_000012.11:g.7945661C>G , CM000674.1:g.7945661C>G GRCh37
NC_000012.10:g.7836928C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000229307.9:c.267C>G MANE Select ENSP00000229307.4:p.Asp89Glu
ENST00000229307.8:c.267C>G ENSP00000229307.4:p.Asp89Glu
ENST00000526286.1:c.267C>G ENSP00000435288.1:p.Asp89Glu
ENST00000526434.2:n.411C>G
ENST00000541267.5:c.195C>G ENSP00000444434.1:p.Asp65Glu
NM_001297698.1:c.267C>G NP_001284627.1:p.Asp89Glu
NM_024865.3:c.267C>G NP_079141.2:p.Asp89Glu
XM_011520850.1:c.267C>G XP_011519152.1:p.Asp89Glu
XM_011520851.1:c.195C>G XP_011519153.1:p.Asp65Glu
XM_011520852.1:c.-106C>G XP_011519154.1:n.-106C>G
NM_024865.4:c.267C>G MANE Select NP_079141.2:p.Asp89Glu
NM_001297698.2:c.267C>G NP_001284627.1:p.Asp89Glu