Canonical Allele Identifier: CA1696262936
Gene: HOXA13 HGNC NCBI

Linked Data

dbSNP Id: rs1784026066
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27198068A>G , CM000669.2:g.27198068A>G GRCh38
NC_000007.13:g.27237687A>G , CM000669.1:g.27237687A>G GRCh37
NC_000007.12:g.27204212A>G NCBI36
NG_008181.1:g.7039T>C
NG_008181.2:g.7039T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000649031.1:c.*130T>C MANE Select ENSP00000497112.1:n.*130T>C
ENST00000222753.5:c.*130T>C ENSP00000222753.4:n.*130T>C
NM_000522.4:c.*130T>C NP_000513.2:n.*130T>C
XM_011515344.1:c.*130T>C XP_011513646.1:n.*130T>C
NM_000522.5:c.*130T>C MANE Select NP_000513.2:n.*130T>C
Search 100 bp 5'
Search 100 bp 3'