Canonical Allele Identifier: CA370605135
Gene: NKX3-1 HGNC NCBI

Linked Data

dbSNP Id: rs757610599
gnomAD v3: 8-23682753-G-C
gnomAD v4: 8-23682753-G-C
MyVariant Identifiers: chr8:g.23540266G>C (hg19) chr8:g.23682753G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23682753G>C , CM000670.2:g.23682753G>C GRCh38
NC_000008.10:g.23540266G>C , CM000670.1:g.23540266G>C GRCh37
NC_000008.9:g.23596211G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000380871.5:c.137C>G MANE Select ENSP00000370253.4:p.Thr46Arg
ENST00000380871.4:c.137C>G ENSP00000370253.4:p.Thr46Arg
ENST00000523261.1:c.33+104C>G ENSP00000429729.1:n.33+104C>G
NM_001256339.1:c.33+104C>G NP_001243268.1:n.33+104C>G
NM_006167.3:c.137C>G NP_006158.2:p.Thr46Arg
NR_046072.1:n.18+151C>G
XR_001745842.1:n.1312+14003G>C
NM_006167.4:c.137C>G MANE Select NP_006158.2:p.Thr46Arg
NR_046072.2:n.35+151C>G
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