Canonical Allele Identifier: CA1906411725
Gene: CXCL12 HGNC NCBI

Linked Data

dbSNP Id: rs1839813331

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.44386115del , CM000672.2:g.44386115del GRCh38
NC_000010.10:g.44881563del , CM000672.1:g.44881563del GRCh37
NC_000010.9:g.44201569del NCBI36
NG_016861.1:g.3985del
NG_016861.2:g.3985del

Transcript Alleles

HGVS Amino-acid Change
ENST00000496375.1:n.381del