Canonical Allele Identifier: CA2263823585
Gene: DLX3 HGNC NCBI

Linked Data

dbSNP Id: rs2278163
gnomAD v4: 17-49995062-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49995062G>C , CM000679.2:g.49995062G>C GRCh38
NC_000017.10:g.48072426G>C , CM000679.1:g.48072426G>C GRCh37
NC_000017.9:g.45427425G>C NCBI36
NG_023063.1:g.5163C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000434704.2:c.-64C>G MANE Select ENSP00000389870.2:n.-64C>G
NM_005220.2:c.-64C>G NP_005211.1:n.-64C>G
XM_011524458.1:c.-64C>G XP_011522760.1:n.-64C>G
NM_005220.3:c.-64C>G MANE Select NP_005211.1:n.-64C>G
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