Canonical Allele Identifier: CA349353139
Gene: HOXD13 HGNC NCBI

Linked Data

dbSNP Id: rs2105379105
MyVariant Identifiers: chr2:g.176958244T>A (hg19) chr2:g.176093516T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.176093516T>A , CM000664.2:g.176093516T>A GRCh38
NC_000002.11:g.176958244T>A , CM000664.1:g.176958244T>A GRCh37
NC_000002.10:g.176666490T>A NCBI36
NG_008137.1:g.5713T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000392539.4:c.626T>A MANE Select ENSP00000376322.3:p.Met209Lys
ENST00000392539.3:c.626T>A ENSP00000376322.3:p.Met209Lys
NM_000523.3:c.626T>A NP_000514.2:p.Met209Lys
XM_011511068.1:c.725-964T>A XP_011509370.1:n.725-964T>A
XM_011511068.2:c.725-964T>A XP_011509370.1:n.725-964T>A
NM_000523.4:c.626T>A MANE Select NP_000514.2:p.Met209Lys
Search 100 bp 5'
Search 100 bp 3'