Canonical Allele Identifier: CA349369450
Gene: HOXD10 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.176983710C>G (hg19) chr2:g.176118982C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176118982C>G , CM000664.2:g.176118982C>G GRCh38
NC_000002.11:g.176983710C>G , CM000664.1:g.176983710C>G GRCh37
NC_000002.10:g.176691956C>G NCBI36
NG_008133.2:g.12219C>G , LRG_246:g.12219C>G
NG_009225.1:g.1298C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000249501.5:c.774C>G MANE Select ENSP00000249501.4:p.Ser258Arg
ENST00000249501.4:c.774C>G ENSP00000249501.4:p.Ser258Arg
ENST00000490088.2:n.598C>G
ENST00000549469.1:n.645C>G
NM_002148.3:c.774C>G , LRG_246t1:c.774C>G NP_002139.2:p.Ser258Arg
NM_002148.4:c.774C>G MANE Select NP_002139.2:p.Ser258Arg
Search 100 bp 5'
Search 100 bp 3'