Canonical Allele Identifier: CA2787788862
Gene: CXCL12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.44386083C>T , CM000672.2:g.44386083C>T GRCh38
NC_000010.10:g.44881531C>T , CM000672.1:g.44881531C>T GRCh37
NC_000010.9:g.44201537C>T NCBI36
NG_016861.1:g.4015G>A
NG_016861.2:g.4015G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000496375.1:n.411G>A