Canonical Allele Identifier: CA1906411638
Gene: CXCL12 HGNC NCBI

Linked Data

dbSNP Id: rs1839810681

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.44386019A>C , CM000672.2:g.44386019A>C GRCh38
NC_000010.10:g.44881467A>C , CM000672.1:g.44881467A>C GRCh37
NC_000010.9:g.44201473A>C NCBI36
NG_016861.1:g.4079T>G
NG_016861.2:g.4079T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000496375.1:n.475T>G