Canonical Allele Identifier: CA400173978
Gene: DLX3 HGNC NCBI

Linked Data

dbSNP Id: rs1402690715

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000434704.2:c.652A>C MANE Select ENSP00000389870.2:p.Thr218Pro
ENST00000512495.2:c.292A>C ENSP00000449976.1:p.Thr98Pro
NM_005220.2:c.652A>C NP_005211.1:p.Thr218Pro
XM_011524458.1:c.516+1671A>C XP_011522760.1:n.516+1671A>C
NM_005220.3:c.652A>C MANE Select NP_005211.1:p.Thr218Pro