Canonical Allele Identifier: CA349369405
Gene: HOXD10 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.176983697A>C (hg19) chr2:g.176118969A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176118969A>C , CM000664.2:g.176118969A>C GRCh38
NC_000002.11:g.176983697A>C , CM000664.1:g.176983697A>C GRCh37
NC_000002.10:g.176691943A>C NCBI36
NG_008133.2:g.12206A>C , LRG_246:g.12206A>C
NG_009225.1:g.1285A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000249501.5:c.761A>C MANE Select ENSP00000249501.4:p.Asp254Ala
ENST00000249501.4:c.761A>C ENSP00000249501.4:p.Asp254Ala
ENST00000490088.2:n.585A>C
ENST00000549469.1:n.632A>C
NM_002148.3:c.761A>C , LRG_246t1:c.761A>C NP_002139.2:p.Asp254Ala
NM_002148.4:c.761A>C MANE Select NP_002139.2:p.Asp254Ala
Search 100 bp 5'
Search 100 bp 3'