Canonical Allele Identifier: CA1906411939
Gene: CXCL12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.44386366G= , CM000672.2:g.44386366G= GRCh38
NC_000010.10:g.44881814G= , CM000672.1:g.44881814G= GRCh37
NC_000010.9:g.44201820G= NCBI36
NG_016861.1:g.3732C=
NG_016861.2:g.3732C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000496375.1:n.128C=