Canonical Allele Identifier: CA349353250
Gene: HOXD13 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.176958295T>G (hg19) chr2:g.176093567T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176093567T>G , CM000664.2:g.176093567T>G GRCh38
NC_000002.11:g.176958295T>G , CM000664.1:g.176958295T>G GRCh37
NC_000002.10:g.176666541T>G NCBI36
NG_008137.1:g.5764T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000392539.4:c.677T>G MANE Select ENSP00000376322.3:p.Met226Arg
ENST00000392539.3:c.677T>G ENSP00000376322.3:p.Met226Arg
NM_000523.3:c.677T>G NP_000514.2:p.Met226Arg
XM_011511068.1:c.725-913T>G XP_011509370.1:n.725-913T>G
XM_011511068.2:c.725-913T>G XP_011509370.1:n.725-913T>G
NM_000523.4:c.677T>G MANE Select NP_000514.2:p.Met226Arg
Search 100 bp 5'
Search 100 bp 3'