Canonical Allele Identifier: CA2608932699
Gene: CXCL12 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.44386349G>T , CM000672.2:g.44386349G>T GRCh38
NC_000010.10:g.44881797G>T , CM000672.1:g.44881797G>T GRCh37
NC_000010.9:g.44201803G>T NCBI36
NG_016861.1:g.3749C>A
NG_016861.2:g.3749C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000496375.1:n.145C>A