Canonical Allele Identifier: CA1906411686
Gene: CXCL12 HGNC NCBI

Linked Data

dbSNP Id: rs1839812536

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.44386082del , CM000672.2:g.44386082del GRCh38
NC_000010.10:g.44881530del , CM000672.1:g.44881530del GRCh37
NC_000010.9:g.44201536del NCBI36
NG_016861.1:g.4017del
NG_016861.2:g.4017del

Transcript Alleles

HGVS Amino-acid Change
ENST00000496375.1:n.413del