Canonical Allele Identifier: CA349369412
Gene: HOXD10 HGNC NCBI

Linked Data

dbSNP Id: rs1689815528
gnomAD v4: 2-176118971-A-G
MyVariant Identifiers: chr2:g.176983699A>G (hg19) chr2:g.176118971A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176118971A>G , CM000664.2:g.176118971A>G GRCh38
NC_000002.11:g.176983699A>G , CM000664.1:g.176983699A>G GRCh37
NC_000002.10:g.176691945A>G NCBI36
NG_008133.2:g.12208A>G , LRG_246:g.12208A>G
NG_009225.1:g.1287A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000249501.5:c.763A>G MANE Select ENSP00000249501.4:p.Thr255Ala
ENST00000249501.4:c.763A>G ENSP00000249501.4:p.Thr255Ala
ENST00000490088.2:n.587A>G
ENST00000549469.1:n.634A>G
NM_002148.3:c.763A>G , LRG_246t1:c.763A>G NP_002139.2:p.Thr255Ala
NM_002148.4:c.763A>G MANE Select NP_002139.2:p.Thr255Ala
Search 100 bp 5'
Search 100 bp 3'