Canonical Allele Identifier: CA1906411972
Gene: CXCL12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.44386428A= , CM000672.2:g.44386428A= GRCh38
NC_000010.10:g.44881876A= , CM000672.1:g.44881876A= GRCh37
NC_000010.9:g.44201882A= NCBI36
NG_016861.1:g.3670T=
NG_016861.2:g.3670T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000496375.1:n.66T=