Canonical Allele Identifier: CA430010867
Gene: HOXD10 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.176983914A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176119186A>G , CM000664.2:g.176119186A>G GRCh38
NC_000002.11:g.176983914A>G , CM000664.1:g.176983914A>G GRCh37
NC_000002.10:g.176692160A>G NCBI36
NG_008133.2:g.12423A>G , LRG_246:g.12423A>G
NG_009225.1:g.1502A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000249501.5:c.978A>G MANE Select ENSP00000249501.4:p.Arg326=
ENST00000249501.4:c.978A>G ENSP00000249501.4:p.Arg326=
ENST00000490088.2:n.802A>G
ENST00000549469.1:n.849A>G
NM_002148.3:c.978A>G , LRG_246t1:c.978A>G NP_002139.2:p.Arg326=
NM_002148.4:c.978A>G MANE Select NP_002139.2:p.Arg326=