Canonical Allele Identifier: CA537772478
Gene: HOXD10 HGNC NCBI

Linked Data

dbSNP Id: rs1190022405
gnomAD v2: 2-176984277-A-G
gnomAD v3: 2-176119549-A-G
gnomAD v4: 2-176119549-A-G
MyVariant Identifiers: chr2:g.176984277A>G (hg19) chr2:g.176119549A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176119549A>G , CM000664.2:g.176119549A>G GRCh38
NC_000002.11:g.176984277A>G , CM000664.1:g.176984277A>G GRCh37
NC_000002.10:g.176692523A>G NCBI36
NG_008133.2:g.12786A>G , LRG_246:g.12786A>G
NG_009225.1:g.1865A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000249501.5:c.*318A>G MANE Select ENSP00000249501.4:n.*318A>G
ENST00000249501.4:c.*318A>G ENSP00000249501.4:n.*318A>G
NM_002148.3:c.*318A>G , LRG_246t1:c.*318A>G NP_002139.2:n.*318A>G
NM_002148.4:c.*318A>G MANE Select NP_002139.2:n.*318A>G
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