Canonical Allele Identifier: CA500989438
Gene: DLX3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.48069199G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49991835G>A , CM000679.2:g.49991835G>A GRCh38
NC_000017.10:g.48069199G>A , CM000679.1:g.48069199G>A GRCh37
NC_000017.9:g.45424198G>A NCBI36
NG_023063.1:g.8390C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000434704.2:c.546C>T MANE Select ENSP00000389870.2:p.Ser182=
ENST00000512495.2:c.186C>T ENSP00000449976.1:p.Ser62=
NM_005220.2:c.546C>T NP_005211.1:p.Ser182=
XM_011524458.1:c.516+1565C>T XP_011522760.1:n.516+1565C>T
NM_005220.3:c.546C>T MANE Select NP_005211.1:p.Ser182=
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