Canonical Allele Identifier: CA592922677

Gene: CXCL12

Linked Data

• dbSNP Id: rs1221874629
• gnomAD v2: 10-44881773-T-C
• gnomAD v3: 10-44386325-T-C
• gnomAD v4: 10-44386325-T-C
• MyVariant Identifiers: chr10:g.44881773T>C (hg19) ; chr10:g.44386325T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.44386325T>C , CM000672.2:g.44386325T>C	GRCh38
NC_000010.10:g.44881773T>C , CM000672.1:g.44881773T>C	GRCh37
NC_000010.9:g.44201779T>C	NCBI36
NG_016861.1:g.3773A>G
NG_016861.2:g.3773A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496375.1:n.169A>G