Canonical Allele Identifier: CA349370754
Gene: HOXD10 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.176983910G>A (hg19) chr2:g.176119182G>A (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000249501.5:c.974G>A MANE Select ENSP00000249501.4:p.Ser325Asn
ENST00000249501.4:c.974G>A ENSP00000249501.4:p.Ser325Asn
ENST00000490088.2:n.798G>A
ENST00000549469.1:n.845G>A
NM_002148.3:c.974G>A , LRG_246t1:c.974G>A NP_002139.2:p.Ser325Asn
NM_002148.4:c.974G>A MANE Select NP_002139.2:p.Ser325Asn
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