Canonical Allele Identifier: CA1906411648
Gene: CXCL12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.44386025A= , CM000672.2:g.44386025A= GRCh38
NC_000010.10:g.44881473A= , CM000672.1:g.44881473A= GRCh37
NC_000010.9:g.44201479A= NCBI36
NG_016861.1:g.4073T=
NG_016861.2:g.4073T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000496375.1:n.469T=