Canonical Allele Identifier: CA927778566
Gene: CXCL12 HGNC NCBI

Linked Data

dbSNP Id: rs1839821304

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.44386382G>T , CM000672.2:g.44386382G>T GRCh38
NC_000010.10:g.44881830G>T , CM000672.1:g.44881830G>T GRCh37
NC_000010.9:g.44201836G>T NCBI36
NG_016861.1:g.3716C>A
NG_016861.2:g.3716C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000496375.1:n.112C>A