Canonical Allele Identifier: CA349370002
Gene: HOXD10 HGNC NCBI

Linked Data

dbSNP Id: rs1377995717
gnomAD v2: 2-176983813-C-T
gnomAD v3: 2-176119085-C-T
gnomAD v4: 2-176119085-C-T
MyVariant Identifiers: chr2:g.176983813C>T (hg19) chr2:g.176119085C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176119085C>T , CM000664.2:g.176119085C>T GRCh38
NC_000002.11:g.176983813C>T , CM000664.1:g.176983813C>T GRCh37
NC_000002.10:g.176692059C>T NCBI36
NG_008133.2:g.12322C>T , LRG_246:g.12322C>T
NG_009225.1:g.1401C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000249501.5:c.877C>T MANE Select ENSP00000249501.4:p.Arg293Cys
ENST00000249501.4:c.877C>T ENSP00000249501.4:p.Arg293Cys
ENST00000490088.2:n.701C>T
ENST00000549469.1:n.748C>T
NM_002148.3:c.877C>T , LRG_246t1:c.877C>T NP_002139.2:p.Arg293Cys
NM_002148.4:c.877C>T MANE Select NP_002139.2:p.Arg293Cys
Search 100 bp 5'
Search 100 bp 3'