Canonical Allele Identifier: CA1906411622
Gene: CXCL12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.44385995A= , CM000672.2:g.44385995A= GRCh38
NC_000010.10:g.44881443A= , CM000672.1:g.44881443A= GRCh37
NC_000010.9:g.44201449A= NCBI36
NG_016861.1:g.4103T=
NG_016861.2:g.4103T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000496375.1:n.499T=