Canonical Allele Identifier: CA460180680
Gene: NKX3-1 HGNC NCBI

Linked Data

gnomAD v4: 8-23682764-T-C
MyVariant Identifiers: chr8:g.23540277T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23682764T>C , CM000670.2:g.23682764T>C GRCh38
NC_000008.10:g.23540277T>C , CM000670.1:g.23540277T>C GRCh37
NC_000008.9:g.23596222T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000380871.5:c.126A>G MANE Select ENSP00000370253.4:p.Gln42=
ENST00000380871.4:c.126A>G ENSP00000370253.4:p.Gln42=
ENST00000523261.1:c.33+93A>G ENSP00000429729.1:n.33+93A>G
NM_001256339.1:c.33+93A>G NP_001243268.1:n.33+93A>G
NM_006167.3:c.126A>G NP_006158.2:p.Gln42=
NR_046072.1:n.18+140A>G
XR_001745842.1:n.1312+14014T>C
NM_006167.4:c.126A>G MANE Select NP_006158.2:p.Gln42=
NR_046072.2:n.35+140A>G
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