Canonical Allele Identifier: CA8640991
Gene: DLX3 HGNC NCBI

Linked Data

dbSNP Id: rs769444646

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49991825T>C , CM000679.2:g.49991825T>C GRCh38
NC_000017.10:g.48069189T>C , CM000679.1:g.48069189T>C GRCh37
NC_000017.9:g.45424188T>C NCBI36
NG_023063.1:g.8400A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000434704.2:c.556A>G MANE Select ENSP00000389870.2:p.Lys186Glu
ENST00000512495.2:c.196A>G ENSP00000449976.1:p.Lys66Glu
NM_005220.2:c.556A>G NP_005211.1:p.Lys186Glu
XM_011524458.1:c.516+1575A>G XP_011522760.1:n.516+1575A>G
NM_005220.3:c.556A>G MANE Select NP_005211.1:p.Lys186Glu