Canonical Allele Identifier: CA1906411741
Gene: CXCL12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.44386120G= , CM000672.2:g.44386120G= GRCh38
NC_000010.10:g.44881568G= , CM000672.1:g.44881568G= GRCh37
NC_000010.9:g.44201574G= NCBI36
NG_016861.1:g.3978C=
NG_016861.2:g.3978C=

Transcript Alleles

HGVS Amino-acid change
ENST00000496375.1:n.374C=