Canonical Allele Identifier: CA383780236
Gene: NANOG HGNC NCBI

Linked Data

dbSNP Id: rs1465537408
gnomAD v2: 12-7945613-A-C
gnomAD v3: 12-7793017-A-C
gnomAD v4: 12-7793017-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.7793017A>C , CM000674.2:g.7793017A>C GRCh38
NC_000012.11:g.7945613A>C , CM000674.1:g.7945613A>C GRCh37
NC_000012.10:g.7836880A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000229307.9:c.219A>C MANE Select ENSP00000229307.4:p.Lys73Asn
ENST00000229307.8:c.219A>C ENSP00000229307.4:p.Lys73Asn
ENST00000526286.1:c.219A>C ENSP00000435288.1:p.Lys73Asn
ENST00000526434.2:n.363A>C
ENST00000541267.5:c.147A>C ENSP00000444434.1:p.Lys49Asn
NM_001297698.1:c.219A>C NP_001284627.1:p.Lys73Asn
NM_024865.3:c.219A>C NP_079141.2:p.Lys73Asn
XM_011520850.1:c.219A>C XP_011519152.1:p.Lys73Asn
XM_011520851.1:c.147A>C XP_011519153.1:p.Lys49Asn
XM_011520852.1:c.-154A>C XP_011519154.1:n.-154A>C
NM_024865.4:c.219A>C MANE Select NP_079141.2:p.Lys73Asn
NM_001297698.2:c.219A>C NP_001284627.1:p.Lys73Asn