Canonical Allele Identifier: CA2263823579
Gene: DLX3 HGNC NCBI

Linked Data

dbSNP Id: rs1906230023
gnomAD v4: 17-49995054-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49995054C>A , CM000679.2:g.49995054C>A GRCh38
NC_000017.10:g.48072418C>A , CM000679.1:g.48072418C>A GRCh37
NC_000017.9:g.45427417C>A NCBI36
NG_023063.1:g.5171G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000434704.2:c.-56G>T MANE Select ENSP00000389870.2:n.-56G>T
NM_005220.2:c.-56G>T NP_005211.1:n.-56G>T
XM_011524458.1:c.-56G>T XP_011522760.1:n.-56G>T
NM_005220.3:c.-56G>T MANE Select NP_005211.1:n.-56G>T
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