Canonical Allele Identifier: CA349353029
Gene: HOXD13 HGNC NCBI

Linked Data

dbSNP Id: rs2105378984
MyVariant Identifiers: chr2:g.176958195T>A (hg19) chr2:g.176093467T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176093467T>A , CM000664.2:g.176093467T>A GRCh38
NC_000002.11:g.176958195T>A , CM000664.1:g.176958195T>A GRCh37
NC_000002.10:g.176666441T>A NCBI36
NG_008137.1:g.5664T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000392539.4:c.577T>A MANE Select ENSP00000376322.3:p.Tyr193Asn
ENST00000392539.3:c.577T>A ENSP00000376322.3:p.Tyr193Asn
NM_000523.3:c.577T>A NP_000514.2:p.Tyr193Asn
XM_011511068.1:c.725-1013T>A XP_011509370.1:n.725-1013T>A
XM_011511068.2:c.725-1013T>A XP_011509370.1:n.725-1013T>A
NM_000523.4:c.577T>A MANE Select NP_000514.2:p.Tyr193Asn
Search 100 bp 5'
Search 100 bp 3'