Canonical Allele Identifier: CA206329655

Gene: CXCL12

Linked Data

• dbSNP Id: rs35144079
• MyVariant Identifiers: chr10:g.44881658del (hg19) ; chr10:g.44386210del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.44386213del , CM000672.2:g.44386213del	GRCh38
NC_000010.10:g.44881661del , CM000672.1:g.44881661del	GRCh37
NC_000010.9:g.44201667del	NCBI36
NG_016861.1:g.3888del
NG_016861.2:g.3888del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496375.1:n.284del