Canonical Allele Identifier: CA2714008056
Gene: HOXA13 HGNC NCBI

Linked Data

dbSNP Id: rs2115470950
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27198169A>T , CM000669.2:g.27198169A>T GRCh38
NC_000007.13:g.27237788A>T , CM000669.1:g.27237788A>T GRCh37
NC_000007.12:g.27204313A>T NCBI36
NG_008181.1:g.6938T>A
NG_008181.2:g.6938T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000649031.1:c.*29T>A MANE Select ENSP00000497112.1:n.*29T>A
ENST00000222753.5:c.*29T>A ENSP00000222753.4:n.*29T>A
NM_000522.4:c.*29T>A NP_000513.2:n.*29T>A
XM_011515344.1:c.*29T>A XP_011513646.1:n.*29T>A
NM_000522.5:c.*29T>A MANE Select NP_000513.2:n.*29T>A
Search 100 bp 5'
Search 100 bp 3'