Canonical Allele Identifier: CA927778390
Gene: CXCL12 HGNC NCBI

Linked Data

dbSNP Id: rs1839808818

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.44385964T>C , CM000672.2:g.44385964T>C GRCh38
NC_000010.10:g.44881412T>C , CM000672.1:g.44881412T>C GRCh37
NC_000010.9:g.44201418T>C NCBI36
NG_016861.1:g.4134A>G
NG_016861.2:g.4134A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000496375.1:n.518+12A>G