Canonical Allele Identifier: CA603171043
Gene: NANOG HGNC NCBI

Linked Data

dbSNP Id: rs1329354640
gnomAD v2: 12-7945327-G-A
MyVariant Identifiers: chr12:g.7945327G>A (hg19) chr12:g.7792731G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.7792731G>A , CM000674.2:g.7792731G>A GRCh38
NC_000012.11:g.7945327G>A , CM000674.1:g.7945327G>A GRCh37
NC_000012.10:g.7836594G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000229307.9:c.152-219G>A MANE Select ENSP00000229307.4:n.152-219G>A
ENST00000229307.8:c.152-219G>A ENSP00000229307.4:n.152-219G>A
ENST00000526286.1:c.152-219G>A ENSP00000435288.1:n.152-219G>A
ENST00000526434.2:n.334-257G>A
ENST00000541267.5:c.80-219G>A ENSP00000444434.1:n.80-219G>A
NM_001297698.1:c.152-219G>A NP_001284627.1:n.152-219G>A
NM_024865.3:c.152-219G>A NP_079141.2:n.152-219G>A
XM_011520850.1:c.152-219G>A XP_011519152.1:n.152-219G>A
XM_011520851.1:c.80-219G>A XP_011519153.1:n.80-219G>A
XM_011520852.1:c.-183-257G>A XP_011519154.1:n.-183-257G>A
NM_024865.4:c.152-219G>A MANE Select NP_079141.2:n.152-219G>A
NM_001297698.2:c.152-219G>A NP_001284627.1:n.152-219G>A
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