Canonical Allele Identifier: CA537975571
Gene: HOXD10 HGNC NCBI

Linked Data

dbSNP Id: rs1338848918

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176118916T>G , CM000664.2:g.176118916T>G GRCh38
NC_000002.11:g.176983644T>G , CM000664.1:g.176983644T>G GRCh37
NC_000002.10:g.176691890T>G NCBI36
NG_008133.2:g.12153T>G , LRG_246:g.12153T>G
NG_009225.1:g.1232T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000249501.5:c.746-38T>G MANE Select ENSP00000249501.4:n.746-38T>G
ENST00000249501.4:c.746-38T>G ENSP00000249501.4:n.746-38T>G
ENST00000490088.2:n.570-38T>G
ENST00000549469.1:n.617-38T>G
NM_002148.3:c.746-38T>G , LRG_246t1:c.746-38T>G NP_002139.2:n.746-38T>G
NM_002148.4:c.746-38T>G MANE Select NP_002139.2:n.746-38T>G