Canonical Allele Identifier: CA430226065
Gene: HOXD10 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.176983815C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176119087C>A , CM000664.2:g.176119087C>A GRCh38
NC_000002.11:g.176983815C>A , CM000664.1:g.176983815C>A GRCh37
NC_000002.10:g.176692061C>A NCBI36
NG_008133.2:g.12324C>A , LRG_246:g.12324C>A
NG_009225.1:g.1403C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000249501.5:c.879C>A MANE Select ENSP00000249501.4:p.Arg293=
ENST00000249501.4:c.879C>A ENSP00000249501.4:p.Arg293=
ENST00000490088.2:n.703C>A
ENST00000549469.1:n.750C>A
NM_002148.3:c.879C>A , LRG_246t1:c.879C>A NP_002139.2:p.Arg293=
NM_002148.4:c.879C>A MANE Select NP_002139.2:p.Arg293=
Search 100 bp 5'
Search 100 bp 3'