Canonical Allele Identifier: CA349353082
Gene: HOXD13 HGNC NCBI

Linked Data

dbSNP Id: rs2105379041
MyVariant Identifiers: chr2:g.176958218C>A (hg19) chr2:g.176093490C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176093490C>A , CM000664.2:g.176093490C>A GRCh38
NC_000002.11:g.176958218C>A , CM000664.1:g.176958218C>A GRCh37
NC_000002.10:g.176666464C>A NCBI36
NG_008137.1:g.5687C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000392539.4:c.600C>A MANE Select ENSP00000376322.3:p.Tyr200Ter
ENST00000392539.3:c.600C>A ENSP00000376322.3:p.Tyr200Ter
NM_000523.3:c.600C>A NP_000514.2:p.Tyr200Ter
XM_011511068.1:c.725-990C>A XP_011509370.1:n.725-990C>A
XM_011511068.2:c.725-990C>A XP_011509370.1:n.725-990C>A
NM_000523.4:c.600C>A MANE Select NP_000514.2:p.Tyr200Ter
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