Canonical Allele Identifier: CA1906411689
Gene: CXCL12 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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