Canonical Allele Identifier: CA430225938
Gene: HOXD10 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.176983704A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176118976A>G , CM000664.2:g.176118976A>G GRCh38
NC_000002.11:g.176983704A>G , CM000664.1:g.176983704A>G GRCh37
NC_000002.10:g.176691950A>G NCBI36
NG_008133.2:g.12213A>G , LRG_246:g.12213A>G
NG_009225.1:g.1292A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000249501.5:c.768A>G MANE Select ENSP00000249501.4:p.Pro256=
ENST00000249501.4:c.768A>G ENSP00000249501.4:p.Pro256=
ENST00000490088.2:n.592A>G
ENST00000549469.1:n.639A>G
NM_002148.3:c.768A>G , LRG_246t1:c.768A>G NP_002139.2:p.Pro256=
NM_002148.4:c.768A>G MANE Select NP_002139.2:p.Pro256=
Search 100 bp 5'
Search 100 bp 3'