Canonical Allele Identifier: CA665410490

Gene: CXCL12

Linked Data

• dbSNP Id: rs1439594534
• gnomAD v3: 10-44386261-G-A
• gnomAD v4: 10-44386261-G-A
• MyVariant Identifiers: chr10:g.44881709G>A (hg19) ; chr10:g.44386261G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.44386261G>A , CM000672.2:g.44386261G>A	GRCh38
NC_000010.10:g.44881709G>A , CM000672.1:g.44881709G>A	GRCh37
NC_000010.9:g.44201715G>A	NCBI36
NG_016861.1:g.3837C>T
NG_016861.2:g.3837C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496375.1:n.233C>T