Canonical Allele Identifier: CA1977433
Gene: HOXD10 HGNC NCBI

Linked Data

dbSNP Id: rs778140250

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176119182G>T , CM000664.2:g.176119182G>T GRCh38
NC_000002.11:g.176983910G>T , CM000664.1:g.176983910G>T GRCh37
NC_000002.10:g.176692156G>T NCBI36
NG_008133.2:g.12419G>T , LRG_246:g.12419G>T
NG_009225.1:g.1498G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000249501.5:c.974G>T MANE Select ENSP00000249501.4:p.Ser325Ile
ENST00000249501.4:c.974G>T ENSP00000249501.4:p.Ser325Ile
ENST00000490088.2:n.798G>T
ENST00000549469.1:n.845G>T
NM_002148.3:c.974G>T , LRG_246t1:c.974G>T NP_002139.2:p.Ser325Ile
NM_002148.4:c.974G>T MANE Select NP_002139.2:p.Ser325Ile