Canonical Allele Identifier: CA537772476
Gene: HOXD10 HGNC NCBI

Linked Data

dbSNP Id: rs1459676732

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176119546C>T , CM000664.2:g.176119546C>T GRCh38
NC_000002.11:g.176984274C>T , CM000664.1:g.176984274C>T GRCh37
NC_000002.10:g.176692520C>T NCBI36
NG_008133.2:g.12783C>T , LRG_246:g.12783C>T
NG_009225.1:g.1862C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000249501.5:c.*315C>T MANE Select ENSP00000249501.4:n.*315C>T
ENST00000249501.4:c.*315C>T ENSP00000249501.4:n.*315C>T
NM_002148.3:c.*315C>T , LRG_246t1:c.*315C>T NP_002139.2:n.*315C>T
NM_002148.4:c.*315C>T MANE Select NP_002139.2:n.*315C>T