Canonical Allele Identifier: CA665410502

Gene: CXCL12

Linked Data

• dbSNP Id: rs1183392782
• gnomAD v3: 10-44386285-G-C
• gnomAD v4: 10-44386285-G-C
• MyVariant Identifiers: chr10:g.44881733G>C (hg19) ; chr10:g.44386285G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.44386285G>C , CM000672.2:g.44386285G>C	GRCh38
NC_000010.10:g.44881733G>C , CM000672.1:g.44881733G>C	GRCh37
NC_000010.9:g.44201739G>C	NCBI36
NG_016861.1:g.3813C>G
NG_016861.2:g.3813C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496375.1:n.209C>G