Canonical Allele Identifier: CA1906411611
Gene: CXCL12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.44385990G= , CM000672.2:g.44385990G= GRCh38
NC_000010.10:g.44881438G= , CM000672.1:g.44881438G= GRCh37
NC_000010.9:g.44201444G= NCBI36
NG_016861.1:g.4108C=
NG_016861.2:g.4108C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000496375.1:n.504C=