Canonical Allele Identifier: CA665410470

Gene: CXCL12

Linked Data

• dbSNP Id: rs1433313212
• gnomAD v3: 10-44386221-C-T
• gnomAD v4: 10-44386221-C-T
• MyVariant Identifiers: chr10:g.44881669C>T (hg19) ; chr10:g.44386221C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.44386221C>T , CM000672.2:g.44386221C>T	GRCh38
NC_000010.10:g.44881669C>T , CM000672.1:g.44881669C>T	GRCh37
NC_000010.9:g.44201675C>T	NCBI36
NG_016861.1:g.3877G>A
NG_016861.2:g.3877G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496375.1:n.273G>A