Canonical Allele Identifier: CA478527569
Gene: NANOG HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.7945703T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.7793107T>G , CM000674.2:g.7793107T>G GRCh38
NC_000012.11:g.7945703T>G , CM000674.1:g.7945703T>G GRCh37
NC_000012.10:g.7836970T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000229307.9:c.309T>G MANE Select ENSP00000229307.4:p.Ser103=
ENST00000229307.8:c.309T>G ENSP00000229307.4:p.Ser103=
ENST00000526286.1:c.309T>G ENSP00000435288.1:p.Ser103=
ENST00000526434.2:n.453T>G
ENST00000541267.5:c.237T>G ENSP00000444434.1:p.Ser79=
NM_001297698.1:c.309T>G NP_001284627.1:p.Ser103=
NM_024865.3:c.309T>G NP_079141.2:p.Ser103=
XM_011520850.1:c.309T>G XP_011519152.1:p.Ser103=
XM_011520851.1:c.237T>G XP_011519153.1:p.Ser79=
XM_011520852.1:c.-64T>G XP_011519154.1:n.-64T>G
NM_024865.4:c.309T>G MANE Select NP_079141.2:p.Ser103=
NM_001297698.2:c.309T>G NP_001284627.1:p.Ser103=