Canonical Allele Identifier: CA349369990
Gene: HOXD10 HGNC NCBI

Linked Data

dbSNP Id: rs1574953740
MyVariant Identifiers: chr2:g.176983810A>C (hg19) chr2:g.176119082A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176119082A>C , CM000664.2:g.176119082A>C GRCh38
NC_000002.11:g.176983810A>C , CM000664.1:g.176983810A>C GRCh37
NC_000002.10:g.176692056A>C NCBI36
NG_008133.2:g.12319A>C , LRG_246:g.12319A>C
NG_009225.1:g.1398A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000249501.5:c.874A>C MANE Select ENSP00000249501.4:p.Thr292Pro
ENST00000249501.4:c.874A>C ENSP00000249501.4:p.Thr292Pro
ENST00000490088.2:n.698A>C
ENST00000549469.1:n.745A>C
NM_002148.3:c.874A>C , LRG_246t1:c.874A>C NP_002139.2:p.Thr292Pro
NM_002148.4:c.874A>C MANE Select NP_002139.2:p.Thr292Pro
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