Canonical Allele Identifier: CA1906411709
Gene: CXCL12 HGNC NCBI

Linked Data

dbSNP Id: rs1839813037

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.44386106T>C , CM000672.2:g.44386106T>C GRCh38
NC_000010.10:g.44881554T>C , CM000672.1:g.44881554T>C GRCh37
NC_000010.9:g.44201560T>C NCBI36
NG_016861.1:g.3992A>G
NG_016861.2:g.3992A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000496375.1:n.388A>G