Canonical Allele Identifier: CA124421
Gene: HOXD10 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 14878
ClinVar RCV Id: RCV000016006
dbSNP Id: rs104893634

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176119164T>A , CM000664.2:g.176119164T>A GRCh38
NC_000002.11:g.176983892T>A , CM000664.1:g.176983892T>A GRCh37
NC_000002.10:g.176692138T>A NCBI36
NG_008133.2:g.12401T>A , LRG_246:g.12401T>A
NG_009225.1:g.1480T>A

Transcript Alleles

HGVS Amino-acid change
NM_002148.3:c.956T>A , LRG_246t1:c.956T>A NP_002139.2:p.Met319Lys
ENST00000249501.4:c.956T>A ENSP00000249501.4:p.Met319Lys
ENST00000490088.2:n.780T>A
ENST00000549469.1:n.827T>A