Canonical Allele Identifier: CA2662046515
Gene: HOXD13 HGNC NCBI

Linked Data

gnomAD v4: 2-176093686-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176093686G>T , CM000664.2:g.176093686G>T GRCh38
NC_000002.11:g.176958414G>T , CM000664.1:g.176958414G>T GRCh37
NC_000002.10:g.176666660G>T NCBI36
NG_008137.1:g.5883G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000392539.4:c.781+15G>T MANE Select ENSP00000376322.3:n.781+15G>T
ENST00000392539.3:c.781+15G>T ENSP00000376322.3:n.781+15G>T
NM_000523.3:c.781+15G>T NP_000514.2:n.781+15G>T
XM_011511068.1:c.725-794G>T XP_011509370.1:n.725-794G>T
XM_011511068.2:c.725-794G>T XP_011509370.1:n.725-794G>T
NM_000523.4:c.781+15G>T MANE Select NP_000514.2:n.781+15G>T
Search 100 bp 5'
Search 100 bp 3'