Canonical Allele Identifier: CA500989330
Gene: DLX3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.48069088A>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49991724A>C , CM000679.2:g.49991724A>C GRCh38
NC_000017.10:g.48069088A>C , CM000679.1:g.48069088A>C GRCh37
NC_000017.9:g.45424087A>C NCBI36
NG_023063.1:g.8501T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000434704.2:c.657T>G MANE Select ENSP00000389870.2:p.Ser219=
ENST00000512495.2:c.297T>G ENSP00000449976.1:p.Ser99=
NM_005220.2:c.657T>G NP_005211.1:p.Ser219=
XM_011524458.1:c.516+1676T>G XP_011522760.1:n.516+1676T>G
NM_005220.3:c.657T>G MANE Select NP_005211.1:p.Ser219=
Search 100 bp 5'
Search 100 bp 3'