Canonical Allele Identifier: CA1906411839
Gene: CXCL12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.44386229G= , CM000672.2:g.44386229G= GRCh38
NC_000010.10:g.44881677G= , CM000672.1:g.44881677G= GRCh37
NC_000010.9:g.44201683G= NCBI36
NG_016861.1:g.3869C=
NG_016861.2:g.3869C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000496375.1:n.265C=