Canonical Allele Identifier: CA4677906
Gene: NKX3-1 HGNC NCBI

Linked Data

dbSNP Id: rs760710802
ExAC: 8:23540315 G / C
gnomAD v2: 8-23540315-G-C
gnomAD v4: 8-23682802-G-C
MyVariant Identifiers: chr8:g.23540315G>C (hg19) chr8:g.23682802G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23682802G>C , CM000670.2:g.23682802G>C GRCh38
NC_000008.10:g.23540315G>C , CM000670.1:g.23540315G>C GRCh37
NC_000008.9:g.23596260G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000380871.5:c.88C>G MANE Select ENSP00000370253.4:p.Leu30Val
ENST00000380871.4:c.88C>G ENSP00000370253.4:p.Leu30Val
ENST00000523261.1:c.33+55C>G ENSP00000429729.1:n.33+55C>G
NM_001256339.1:c.33+55C>G NP_001243268.1:n.33+55C>G
NM_006167.3:c.88C>G NP_006158.2:p.Leu30Val
NR_046072.1:n.18+102C>G
XR_001745842.1:n.1312+14052G>C
NM_006167.4:c.88C>G MANE Select NP_006158.2:p.Leu30Val
NR_046072.2:n.35+102C>G
Search 100 bp 5'
Search 100 bp 3'