Canonical Allele Identifier: CA626477337
Gene: DLX3 HGNC NCBI

Linked Data

dbSNP Id: rs150591955
gnomAD v2: 17-48072494-G-C
gnomAD v3: 17-49995130-G-C
gnomAD v4: 17-49995130-G-C
MyVariant Identifiers: chr17:g.48072494G>C (hg19) chr17:g.49995130G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49995130G>C , CM000679.2:g.49995130G>C GRCh38
NC_000017.10:g.48072494G>C , CM000679.1:g.48072494G>C GRCh37
NC_000017.9:g.45427493G>C NCBI36
NG_023063.1:g.5095C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000434704.2:c.-132C>G MANE Select ENSP00000389870.2:n.-132C>G
NM_005220.2:c.-132C>G NP_005211.1:n.-132C>G
XM_011524458.1:c.-132C>G XP_011522760.1:n.-132C>G
NM_005220.3:c.-132C>G MANE Select NP_005211.1:n.-132C>G
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