Canonical Allele Identifier: CA349370762
Gene: HOXD10 HGNC NCBI

Linked Data

dbSNP Id: rs1401258981
gnomAD v2: 2-176983913-G-A
gnomAD v4: 2-176119185-G-A
MyVariant Identifiers: chr2:g.176983913G>A (hg19) chr2:g.176119185G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176119185G>A , CM000664.2:g.176119185G>A GRCh38
NC_000002.11:g.176983913G>A , CM000664.1:g.176983913G>A GRCh37
NC_000002.10:g.176692159G>A NCBI36
NG_008133.2:g.12422G>A , LRG_246:g.12422G>A
NG_009225.1:g.1501G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000249501.5:c.977G>A MANE Select ENSP00000249501.4:p.Arg326Gln
ENST00000249501.4:c.977G>A ENSP00000249501.4:p.Arg326Gln
ENST00000490088.2:n.801G>A
ENST00000549469.1:n.848G>A
NM_002148.3:c.977G>A , LRG_246t1:c.977G>A NP_002139.2:p.Arg326Gln
NM_002148.4:c.977G>A MANE Select NP_002139.2:p.Arg326Gln
Search 100 bp 5'
Search 100 bp 3'