Canonical Allele Identifier: CA1977422
Gene: HOXD10 HGNC NCBI

Linked Data

dbSNP Id: rs774941661
ExAC: 2:176983815 C / T
gnomAD v2: 2-176983815-C-T
gnomAD v3: 2-176119087-C-T
gnomAD v4: 2-176119087-C-T
COSMIC: COSM4691028
MyVariant Identifiers: chr2:g.176983815C>T (hg19) chr2:g.176119087C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176119087C>T , CM000664.2:g.176119087C>T GRCh38
NC_000002.11:g.176983815C>T , CM000664.1:g.176983815C>T GRCh37
NC_000002.10:g.176692061C>T NCBI36
NG_008133.2:g.12324C>T , LRG_246:g.12324C>T
NG_009225.1:g.1403C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000249501.5:c.879C>T MANE Select ENSP00000249501.4:p.Arg293=
ENST00000249501.4:c.879C>T ENSP00000249501.4:p.Arg293=
ENST00000490088.2:n.703C>T
ENST00000549469.1:n.750C>T
NM_002148.3:c.879C>T , LRG_246t1:c.879C>T NP_002139.2:p.Arg293=
NM_002148.4:c.879C>T MANE Select NP_002139.2:p.Arg293=
Search 100 bp 5'
Search 100 bp 3'