Canonical Allele Identifier: CA537772474
Gene: HOXD10 HGNC NCBI

Linked Data

dbSNP Id: rs1242200927

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176119525G>A , CM000664.2:g.176119525G>A GRCh38
NC_000002.11:g.176984253G>A , CM000664.1:g.176984253G>A GRCh37
NC_000002.10:g.176692499G>A NCBI36
NG_008133.2:g.12762G>A , LRG_246:g.12762G>A
NG_009225.1:g.1841G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000249501.5:c.*294G>A MANE Select ENSP00000249501.4:n.*294G>A
ENST00000249501.4:c.*294G>A ENSP00000249501.4:n.*294G>A
NM_002148.3:c.*294G>A , LRG_246t1:c.*294G>A NP_002139.2:n.*294G>A
NM_002148.4:c.*294G>A MANE Select NP_002139.2:n.*294G>A