Canonical Allele Identifier: CA232550005
Gene: NANOG HGNC NCBI

Linked Data

dbSNP Id: rs199844601
gnomAD v2: 12-7945606-G-A
gnomAD v3: 12-7793010-G-A
gnomAD v4: 12-7793010-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.7793010G>A , CM000674.2:g.7793010G>A GRCh38
NC_000012.11:g.7945606G>A , CM000674.1:g.7945606G>A GRCh37
NC_000012.10:g.7836873G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000229307.9:c.212G>A MANE Select ENSP00000229307.4:p.Ser71Asn
ENST00000229307.8:c.212G>A ENSP00000229307.4:p.Ser71Asn
ENST00000526286.1:c.212G>A ENSP00000435288.1:p.Ser71Asn
ENST00000526434.2:n.356G>A
ENST00000541267.5:c.140G>A ENSP00000444434.1:p.Ser47Asn
NM_001297698.1:c.212G>A NP_001284627.1:p.Ser71Asn
NM_024865.3:c.212G>A NP_079141.2:p.Ser71Asn
XM_011520850.1:c.212G>A XP_011519152.1:p.Ser71Asn
XM_011520851.1:c.140G>A XP_011519153.1:p.Ser47Asn
XM_011520852.1:c.-161G>A XP_011519154.1:n.-161G>A
NM_024865.4:c.212G>A MANE Select NP_079141.2:p.Ser71Asn
NM_001297698.2:c.212G>A NP_001284627.1:p.Ser71Asn