Canonical Allele Identifier: CA1906411631
Gene: CXCL12 HGNC NCBI

Linked Data

dbSNP Id: rs1839810409

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.44386018dup , CM000672.2:g.44386018dup GRCh38
NC_000010.10:g.44881466dup , CM000672.1:g.44881466dup GRCh37
NC_000010.9:g.44201472dup NCBI36
NG_016861.1:g.4084dup
NG_016861.2:g.4084dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000496375.1:n.480dup