Canonical Allele Identifier: CA349369390
Gene: HOXD10 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.176983693T>A (hg19) chr2:g.176118965T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176118965T>A , CM000664.2:g.176118965T>A GRCh38
NC_000002.11:g.176983693T>A , CM000664.1:g.176983693T>A GRCh37
NC_000002.10:g.176691939T>A NCBI36
NG_008133.2:g.12202T>A , LRG_246:g.12202T>A
NG_009225.1:g.1281T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000249501.5:c.757T>A MANE Select ENSP00000249501.4:p.Ser253Thr
ENST00000249501.4:c.757T>A ENSP00000249501.4:p.Ser253Thr
ENST00000490088.2:n.581T>A
ENST00000549469.1:n.628T>A
NM_002148.3:c.757T>A , LRG_246t1:c.757T>A NP_002139.2:p.Ser253Thr
NM_002148.4:c.757T>A MANE Select NP_002139.2:p.Ser253Thr
Search 100 bp 5'
Search 100 bp 3'