Canonical Allele Identifier: CA349369420
Gene: HOXD10 HGNC NCBI

Linked Data

dbSNP Id: rs1351143930
MyVariant Identifiers: chr2:g.176983702C>A (hg19) chr2:g.176118974C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176118974C>A , CM000664.2:g.176118974C>A GRCh38
NC_000002.11:g.176983702C>A , CM000664.1:g.176983702C>A GRCh37
NC_000002.10:g.176691948C>A NCBI36
NG_008133.2:g.12211C>A , LRG_246:g.12211C>A
NG_009225.1:g.1290C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000249501.5:c.766C>A MANE Select ENSP00000249501.4:p.Pro256Thr
ENST00000249501.4:c.766C>A ENSP00000249501.4:p.Pro256Thr
ENST00000490088.2:n.590C>A
ENST00000549469.1:n.637C>A
NM_002148.3:c.766C>A , LRG_246t1:c.766C>A NP_002139.2:p.Pro256Thr
NM_002148.4:c.766C>A MANE Select NP_002139.2:p.Pro256Thr
Search 100 bp 5'
Search 100 bp 3'