Canonical Allele Identifier: CA349369975
Gene: HOXD10 HGNC NCBI

Linked Data

gnomAD v4: 2-176119078-C-A
MyVariant Identifiers: chr2:g.176983806C>A (hg19) chr2:g.176119078C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176119078C>A , CM000664.2:g.176119078C>A GRCh38
NC_000002.11:g.176983806C>A , CM000664.1:g.176983806C>A GRCh37
NC_000002.10:g.176692052C>A NCBI36
NG_008133.2:g.12315C>A , LRG_246:g.12315C>A
NG_009225.1:g.1394C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000249501.5:c.870C>A MANE Select ENSP00000249501.4:p.Tyr290Ter
ENST00000249501.4:c.870C>A ENSP00000249501.4:p.Tyr290Ter
ENST00000490088.2:n.694C>A
ENST00000549469.1:n.741C>A
NM_002148.3:c.870C>A , LRG_246t1:c.870C>A NP_002139.2:p.Tyr290Ter
NM_002148.4:c.870C>A MANE Select NP_002139.2:p.Tyr290Ter
Search 100 bp 5'
Search 100 bp 3'