Canonical Allele Identifier: CA349370750
Gene: HOXD10 HGNC NCBI

Linked Data

gnomAD v4: 2-176119180-G-A
MyVariant Identifiers: chr2:g.176983908G>A (hg19) chr2:g.176119180G>A (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000249501.5:c.972G>A MANE Select ENSP00000249501.4:p.Met324Ile
ENST00000249501.4:c.972G>A ENSP00000249501.4:p.Met324Ile
ENST00000490088.2:n.796G>A
ENST00000549469.1:n.843G>A
NM_002148.3:c.972G>A , LRG_246t1:c.972G>A NP_002139.2:p.Met324Ile
NM_002148.4:c.972G>A MANE Select NP_002139.2:p.Met324Ile
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Search 100 bp 3'