Canonical Allele Identifier: CA400174727
Gene: DLX3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.48069195A>C (hg19) chr17:g.49991831A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49991831A>C , CM000679.2:g.49991831A>C GRCh38
NC_000017.10:g.48069195A>C , CM000679.1:g.48069195A>C GRCh37
NC_000017.9:g.45424194A>C NCBI36
NG_023063.1:g.8394T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000434704.2:c.550T>G MANE Select ENSP00000389870.2:p.Phe184Val
ENST00000512495.2:c.190T>G ENSP00000449976.1:p.Phe64Val
NM_005220.2:c.550T>G NP_005211.1:p.Phe184Val
XM_011524458.1:c.516+1569T>G XP_011522760.1:n.516+1569T>G
NM_005220.3:c.550T>G MANE Select NP_005211.1:p.Phe184Val
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