Canonical Allele Identifier: CA1906411832
Gene: CXCL12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.44386213C= , CM000672.2:g.44386213C= GRCh38
NC_000010.10:g.44881661C= , CM000672.1:g.44881661C= GRCh37
NC_000010.9:g.44201667C= NCBI36
NG_016861.1:g.3885G=
NG_016861.2:g.3885G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000496375.1:n.281G=