Canonical Allele Identifier: CA1977420
Gene: HOXD10 HGNC NCBI

Linked Data

dbSNP Id: rs745467585

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000249501.5:c.870C>T MANE Select ENSP00000249501.4:p.Tyr290=
ENST00000249501.4:c.870C>T ENSP00000249501.4:p.Tyr290=
ENST00000490088.2:n.694C>T
ENST00000549469.1:n.741C>T
NM_002148.3:c.870C>T , LRG_246t1:c.870C>T NP_002139.2:p.Tyr290=
NM_002148.4:c.870C>T MANE Select NP_002139.2:p.Tyr290=