Canonical Allele Identifier: CA206329584

Gene: CXCL12

Linked Data

• dbSNP Id: rs1022948025
• gnomAD v4: 10-44386080-C-A
• MyVariant Identifiers: chr10:g.44881528C>A (hg19) ; chr10:g.44386080C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.44386080C>A , CM000672.2:g.44386080C>A	GRCh38
NC_000010.10:g.44881528C>A , CM000672.1:g.44881528C>A	GRCh37
NC_000010.9:g.44201534C>A	NCBI36
NG_016861.1:g.4018G>T
NG_016861.2:g.4018G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496375.1:n.414G>T