Canonical Allele Identifier: CA460180767
Gene: NKX3-1 HGNC NCBI

Linked Data

dbSNP Id: rs1164340955
gnomAD v2: 8-23540322-C-A
gnomAD v3: 8-23682809-C-A
gnomAD v4: 8-23682809-C-A
MyVariant Identifiers: chr8:g.23540322C>A (hg19) chr8:g.23682809C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23682809C>A , CM000670.2:g.23682809C>A GRCh38
NC_000008.10:g.23540322C>A , CM000670.1:g.23540322C>A GRCh37
NC_000008.9:g.23596267C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000380871.5:c.81G>T MANE Select ENSP00000370253.4:p.Thr27=
ENST00000380871.4:c.81G>T ENSP00000370253.4:p.Thr27=
ENST00000523261.1:c.33+48G>T ENSP00000429729.1:n.33+48G>T
NM_001256339.1:c.33+48G>T NP_001243268.1:n.33+48G>T
NM_006167.3:c.81G>T NP_006158.2:p.Thr27=
NR_046072.1:n.18+95G>T
XR_001745842.1:n.1312+14059C>A
NM_006167.4:c.81G>T MANE Select NP_006158.2:p.Thr27=
NR_046072.2:n.35+95G>T
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