Canonical Allele Identifier: CA430226062
Gene: HOXD10 HGNC NCBI

Linked Data

dbSNP Id: rs1019848667
gnomAD v2: 2-176983812-C-G
gnomAD v3: 2-176119084-C-G
gnomAD v4: 2-176119084-C-G
MyVariant Identifiers: chr2:g.176983812C>G (hg19) chr2:g.176119084C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176119084C>G , CM000664.2:g.176119084C>G GRCh38
NC_000002.11:g.176983812C>G , CM000664.1:g.176983812C>G GRCh37
NC_000002.10:g.176692058C>G NCBI36
NG_008133.2:g.12321C>G , LRG_246:g.12321C>G
NG_009225.1:g.1400C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000249501.5:c.876C>G MANE Select ENSP00000249501.4:p.Thr292=
ENST00000249501.4:c.876C>G ENSP00000249501.4:p.Thr292=
ENST00000490088.2:n.700C>G
ENST00000549469.1:n.747C>G
NM_002148.3:c.876C>G , LRG_246t1:c.876C>G NP_002139.2:p.Thr292=
NM_002148.4:c.876C>G MANE Select NP_002139.2:p.Thr292=
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