Canonical Allele Identifier: CA400173972
Gene: DLX3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.48069093T>A (hg19) chr17:g.49991729T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49991729T>A , CM000679.2:g.49991729T>A GRCh38
NC_000017.10:g.48069093T>A , CM000679.1:g.48069093T>A GRCh37
NC_000017.9:g.45424092T>A NCBI36
NG_023063.1:g.8496A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000434704.2:c.652A>T MANE Select ENSP00000389870.2:p.Thr218Ser
ENST00000512495.2:c.292A>T ENSP00000449976.1:p.Thr98Ser
NM_005220.2:c.652A>T NP_005211.1:p.Thr218Ser
XM_011524458.1:c.516+1671A>T XP_011522760.1:n.516+1671A>T
NM_005220.3:c.652A>T MANE Select NP_005211.1:p.Thr218Ser
Search 100 bp 5'
Search 100 bp 3'