Canonical Allele Identifier: CA927778589
Gene: CXCL12 HGNC NCBI

Linked Data

dbSNP Id: rs1839822310

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.44386460C>A , CM000672.2:g.44386460C>A GRCh38
NC_000010.10:g.44881908C>A , CM000672.1:g.44881908C>A GRCh37
NC_000010.9:g.44201914C>A NCBI36
NG_016861.1:g.3638G>T
NG_016861.2:g.3638G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000496375.1:n.34G>T