Canonical Allele Identifier: CA349370748
Gene: HOXD10 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.176983908G>T (hg19) chr2:g.176119180G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176119180G>T , CM000664.2:g.176119180G>T GRCh38
NC_000002.11:g.176983908G>T , CM000664.1:g.176983908G>T GRCh37
NC_000002.10:g.176692154G>T NCBI36
NG_008133.2:g.12417G>T , LRG_246:g.12417G>T
NG_009225.1:g.1496G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000249501.5:c.972G>T MANE Select ENSP00000249501.4:p.Met324Ile
ENST00000249501.4:c.972G>T ENSP00000249501.4:p.Met324Ile
ENST00000490088.2:n.796G>T
ENST00000549469.1:n.843G>T
NM_002148.3:c.972G>T , LRG_246t1:c.972G>T NP_002139.2:p.Met324Ile
NM_002148.4:c.972G>T MANE Select NP_002139.2:p.Met324Ile
Search 100 bp 5'
Search 100 bp 3'