Canonical Allele Identifier: CA4677928
Gene: NKX3-1 HGNC NCBI

Linked Data

dbSNP Id: rs11781886
gnomAD v2: 8-23540417-C-T
gnomAD v3: 8-23682904-C-T
gnomAD v4: 8-23682904-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23682904C>T , CM000670.2:g.23682904C>T GRCh38
NC_000008.10:g.23540417C>T , CM000670.1:g.23540417C>T GRCh37
NC_000008.9:g.23596362C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000380871.5:c.-15G>A MANE Select ENSP00000370253.4:n.-15G>A
ENST00000380871.4:c.-15G>A ENSP00000370253.4:n.-15G>A
NM_006167.3:c.-15G>A NP_006158.2:n.-15G>A
NR_046072.1:n.18G>A
XR_001745842.1:n.1312+14154C>T
NM_006167.4:c.-15G>A MANE Select NP_006158.2:n.-15G>A
NR_046072.2:n.35G>A