Canonical Allele Identifier: CA2721709239
Gene: CXCL12 HGNC NCBI

Linked Data

dbSNP Id: rs2132058329

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.44386013del , CM000672.2:g.44386013del GRCh38
NC_000010.10:g.44881461del , CM000672.1:g.44881461del GRCh37
NC_000010.9:g.44201467del NCBI36
NG_016861.1:g.4085del
NG_016861.2:g.4085del

Transcript Alleles

HGVS Amino-acid Change
ENST00000496375.1:n.481del