Canonical Allele Identifier: CA400174723
Gene: DLX3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.48069193G>C (hg19) chr17:g.49991829G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49991829G>C , CM000679.2:g.49991829G>C GRCh38
NC_000017.10:g.48069193G>C , CM000679.1:g.48069193G>C GRCh37
NC_000017.9:g.45424192G>C NCBI36
NG_023063.1:g.8396C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000434704.2:c.552C>G MANE Select ENSP00000389870.2:p.Phe184Leu
ENST00000512495.2:c.192C>G ENSP00000449976.1:p.Phe64Leu
NM_005220.2:c.552C>G NP_005211.1:p.Phe184Leu
XM_011524458.1:c.516+1571C>G XP_011522760.1:n.516+1571C>G
NM_005220.3:c.552C>G MANE Select NP_005211.1:p.Phe184Leu
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