Canonical Allele Identifier: CA1906411931
Gene: CXCL12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.44386365G= , CM000672.2:g.44386365G= GRCh38
NC_000010.10:g.44881813G= , CM000672.1:g.44881813G= GRCh37
NC_000010.9:g.44201819G= NCBI36
NG_016861.1:g.3733C=
NG_016861.2:g.3733C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000496375.1:n.129C=