Canonical Allele Identifier: CA430010882
Gene: HOXD10 HGNC NCBI

Linked Data

dbSNP Id: rs1480877692
gnomAD v3: 2-176119189-G-A
gnomAD v4: 2-176119189-G-A
MyVariant Identifiers: chr2:g.176983917G>A (hg19) chr2:g.176119189G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176119189G>A , CM000664.2:g.176119189G>A GRCh38
NC_000002.11:g.176983917G>A , CM000664.1:g.176983917G>A GRCh37
NC_000002.10:g.176692163G>A NCBI36
NG_008133.2:g.12426G>A , LRG_246:g.12426G>A
NG_009225.1:g.1505G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000249501.5:c.981G>A MANE Select ENSP00000249501.4:p.Glu327=
ENST00000249501.4:c.981G>A ENSP00000249501.4:p.Glu327=
ENST00000490088.2:n.805G>A
ENST00000549469.1:n.852G>A
NM_002148.3:c.981G>A , LRG_246t1:c.981G>A NP_002139.2:p.Glu327=
NM_002148.4:c.981G>A MANE Select NP_002139.2:p.Glu327=
Search 100 bp 5'
Search 100 bp 3'