Canonical Allele Identifier: CA400174735
Gene: DLX3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.48069197T>G (hg19) chr17:g.49991833T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49991833T>G , CM000679.2:g.49991833T>G GRCh38
NC_000017.10:g.48069197T>G , CM000679.1:g.48069197T>G GRCh37
NC_000017.9:g.45424196T>G NCBI36
NG_023063.1:g.8392A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000434704.2:c.548A>C MANE Select ENSP00000389870.2:p.Lys183Thr
ENST00000512495.2:c.188A>C ENSP00000449976.1:p.Lys63Thr
NM_005220.2:c.548A>C NP_005211.1:p.Lys183Thr
XM_011524458.1:c.516+1567A>C XP_011522760.1:n.516+1567A>C
NM_005220.3:c.548A>C MANE Select NP_005211.1:p.Lys183Thr
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