Canonical Allele Identifier: CA2638669142
Gene: DLX3 HGNC NCBI

Linked Data

gnomAD v4: 17-49995139-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49995139G>T , CM000679.2:g.49995139G>T GRCh38
NC_000017.10:g.48072503G>T , CM000679.1:g.48072503G>T GRCh37
NC_000017.9:g.45427502G>T NCBI36
NG_023063.1:g.5086C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000434704.2:c.-141C>A MANE Select ENSP00000389870.2:n.-141C>A
NM_005220.2:c.-141C>A NP_005211.1:n.-141C>A
XM_011524458.1:c.-141C>A XP_011522760.1:n.-141C>A
NM_005220.3:c.-141C>A MANE Select NP_005211.1:n.-141C>A
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