Canonical Allele Identifier: CA460180816
Gene: NKX3-1 HGNC NCBI

Linked Data

dbSNP Id: rs377154556
gnomAD v4: 8-23682833-C-T
MyVariant Identifiers: chr8:g.23540346C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23682833C>T , CM000670.2:g.23682833C>T GRCh38
NC_000008.10:g.23540346C>T , CM000670.1:g.23540346C>T GRCh37
NC_000008.9:g.23596291C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000380871.5:c.57G>A MANE Select ENSP00000370253.4:p.Pro19=
ENST00000380871.4:c.57G>A ENSP00000370253.4:p.Pro19=
ENST00000523261.1:c.33+24G>A ENSP00000429729.1:n.33+24G>A
NM_001256339.1:c.33+24G>A NP_001243268.1:n.33+24G>A
NM_006167.3:c.57G>A NP_006158.2:p.Pro19=
NR_046072.1:n.18+71G>A
XR_001745842.1:n.1312+14083C>T
NM_006167.4:c.57G>A MANE Select NP_006158.2:p.Pro19=
NR_046072.2:n.35+71G>A