Canonical Allele Identifier: CA1906411606
Gene: CXCL12 HGNC NCBI

Linked Data

dbSNP Id: rs1839809280

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.44385983A>C , CM000672.2:g.44385983A>C GRCh38
NC_000010.10:g.44881431A>C , CM000672.1:g.44881431A>C GRCh37
NC_000010.9:g.44201437A>C NCBI36
NG_016861.1:g.4115T>G
NG_016861.2:g.4115T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000496375.1:n.511T>G