Canonical Allele Identifier: CA8641135
Gene: DLX3 HGNC NCBI

Linked Data

dbSNP Id: rs780565504
ExAC: 17:48072405 G / T
gnomAD v2: 17-48072405-G-T
gnomAD v3: 17-49995041-G-T
gnomAD v4: 17-49995041-G-T
MyVariant Identifiers: chr17:g.48072405G>T (hg19) chr17:g.49995041G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49995041G>T , CM000679.2:g.49995041G>T GRCh38
NC_000017.10:g.48072405G>T , CM000679.1:g.48072405G>T GRCh37
NC_000017.9:g.45427404G>T NCBI36
NG_023063.1:g.5184C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000434704.2:c.-43C>A MANE Select ENSP00000389870.2:n.-43C>A
NM_005220.2:c.-43C>A NP_005211.1:n.-43C>A
XM_011524458.1:c.-43C>A XP_011522760.1:n.-43C>A
NM_005220.3:c.-43C>A MANE Select NP_005211.1:n.-43C>A
Search 100 bp 5'
Search 100 bp 3'