Canonical Allele Identifier: CA400174000
Gene: DLX3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.48069096C>T (hg19) chr17:g.49991732C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49991732C>T , CM000679.2:g.49991732C>T GRCh38
NC_000017.10:g.48069096C>T , CM000679.1:g.48069096C>T GRCh37
NC_000017.9:g.45424095C>T NCBI36
NG_023063.1:g.8493G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000434704.2:c.649G>A MANE Select ENSP00000389870.2:p.Asp217Asn
ENST00000512495.2:c.289G>A ENSP00000449976.1:p.Asp97Asn
NM_005220.2:c.649G>A NP_005211.1:p.Asp217Asn
XM_011524458.1:c.516+1668G>A XP_011522760.1:n.516+1668G>A
NM_005220.3:c.649G>A MANE Select NP_005211.1:p.Asp217Asn
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