Canonical Allele Identifier: CA430224618
Gene: HOXD13 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.176958263C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176093535C>G , CM000664.2:g.176093535C>G GRCh38
NC_000002.11:g.176958263C>G , CM000664.1:g.176958263C>G GRCh37
NC_000002.10:g.176666509C>G NCBI36
NG_008137.1:g.5732C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000392539.4:c.645C>G MANE Select ENSP00000376322.3:p.Ser215=
ENST00000392539.3:c.645C>G ENSP00000376322.3:p.Ser215=
NM_000523.3:c.645C>G NP_000514.2:p.Ser215=
XM_011511068.1:c.725-945C>G XP_011509370.1:n.725-945C>G
XM_011511068.2:c.725-945C>G XP_011509370.1:n.725-945C>G
NM_000523.4:c.645C>G MANE Select NP_000514.2:p.Ser215=
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