Canonical Allele Identifier: CA10611956
Gene: HOXD10 HGNC NCBI

Linked Data

ClinVar Variation Id: 332505
ClinVar RCV Id: RCV000278753 RCV003437060
dbSNP Id: rs532592274
gnomAD v2: 2-176984427-A-T
gnomAD v3: 2-176119699-A-T
gnomAD v4: 2-176119699-A-T
COSMIC: COSN23555508
MyVariant Identifiers: chr2:g.176984427A>T (hg19) chr2:g.176119699A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176119699A>T , CM000664.2:g.176119699A>T GRCh38
NC_000002.11:g.176984427A>T , CM000664.1:g.176984427A>T GRCh37
NC_000002.10:g.176692673A>T NCBI36
NG_008133.2:g.12936A>T , LRG_246:g.12936A>T
NG_009225.1:g.2015A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000249501.5:c.*468A>T MANE Select ENSP00000249501.4:n.*468A>T
ENST00000249501.4:c.*468A>T ENSP00000249501.4:n.*468A>T
NM_002148.3:c.*468A>T , LRG_246t1:c.*468A>T NP_002139.2:n.*468A>T
NM_002148.4:c.*468A>T MANE Select NP_002139.2:n.*468A>T
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