Canonical Allele Identifier: CA1906385997
Community Standard Title: NC_000010.11:g.44318290T=
Gene: CXCL12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.44318290T= , CM000672.2:g.44318290T= GRCh38
NC_000010.10:g.44813738T= , CM000672.1:g.44813738T= GRCh37
NC_000010.9:g.44133744T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001747171.1:n.332-20393A=
XR_001747172.1:n.332-20393A=
XR_001747173.1:n.332-20393A=
XR_001747174.1:n.332-20393A=
XR_945912.1:n.311-20393A=