Canonical Allele Identifier: CA349369430
Gene: HOXD10 HGNC NCBI

Linked Data

gnomAD v4: 2-176118977-A-G
MyVariant Identifiers: chr2:g.176983705A>G (hg19) chr2:g.176118977A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176118977A>G , CM000664.2:g.176118977A>G GRCh38
NC_000002.11:g.176983705A>G , CM000664.1:g.176983705A>G GRCh37
NC_000002.10:g.176691951A>G NCBI36
NG_008133.2:g.12214A>G , LRG_246:g.12214A>G
NG_009225.1:g.1293A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000249501.5:c.769A>G MANE Select ENSP00000249501.4:p.Thr257Ala
ENST00000249501.4:c.769A>G ENSP00000249501.4:p.Thr257Ala
ENST00000490088.2:n.593A>G
ENST00000549469.1:n.640A>G
NM_002148.3:c.769A>G , LRG_246t1:c.769A>G NP_002139.2:p.Thr257Ala
NM_002148.4:c.769A>G MANE Select NP_002139.2:p.Thr257Ala
Search 100 bp 5'
Search 100 bp 3'