Canonical Allele Identifier: CA1906411866
Gene: CXCL12 HGNC NCBI

Linked Data

dbSNP Id: rs1839817156

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.44386263C>T , CM000672.2:g.44386263C>T GRCh38
NC_000010.10:g.44881711C>T , CM000672.1:g.44881711C>T GRCh37
NC_000010.9:g.44201717C>T NCBI36
NG_016861.1:g.3835G>A
NG_016861.2:g.3835G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000496375.1:n.231G>A