Canonical Allele Identifier: CA349370761
Gene: HOXD10 HGNC NCBI

Linked Data

gnomAD v4: 2-176119185-G-C
MyVariant Identifiers: chr2:g.176983913G>C (hg19) chr2:g.176119185G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176119185G>C , CM000664.2:g.176119185G>C GRCh38
NC_000002.11:g.176983913G>C , CM000664.1:g.176983913G>C GRCh37
NC_000002.10:g.176692159G>C NCBI36
NG_008133.2:g.12422G>C , LRG_246:g.12422G>C
NG_009225.1:g.1501G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000249501.5:c.977G>C MANE Select ENSP00000249501.4:p.Arg326Pro
ENST00000249501.4:c.977G>C ENSP00000249501.4:p.Arg326Pro
ENST00000490088.2:n.801G>C
ENST00000549469.1:n.848G>C
NM_002148.3:c.977G>C , LRG_246t1:c.977G>C NP_002139.2:p.Arg326Pro
NM_002148.4:c.977G>C MANE Select NP_002139.2:p.Arg326Pro
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