Canonical Allele Identifier: CA500989324
Gene: DLX3 HGNC NCBI

Linked Data

dbSNP Id: rs1906097949
MyVariant Identifiers: chr17:g.48069085G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49991721G>T , CM000679.2:g.49991721G>T GRCh38
NC_000017.10:g.48069085G>T , CM000679.1:g.48069085G>T GRCh37
NC_000017.9:g.45424084G>T NCBI36
NG_023063.1:g.8504C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000434704.2:c.660C>A MANE Select ENSP00000389870.2:p.Ser220=
ENST00000512495.2:c.300C>A ENSP00000449976.1:p.Ser100=
NM_005220.2:c.660C>A NP_005211.1:p.Ser220=
XM_011524458.1:c.516+1679C>A XP_011522760.1:n.516+1679C>A
NM_005220.3:c.660C>A MANE Select NP_005211.1:p.Ser220=
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