Canonical Allele Identifier: CA665410359

Gene: CXCL12

Linked Data

• dbSNP Id: rs1275545654
• MyVariant Identifiers: chr10:g.44881500G>A (hg19) ; chr10:g.44386052G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.44386052G>A , CM000672.2:g.44386052G>A	GRCh38
NC_000010.10:g.44881500G>A , CM000672.1:g.44881500G>A	GRCh37
NC_000010.9:g.44201506G>A	NCBI36
NG_016861.1:g.4046C>T
NG_016861.2:g.4046C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496375.1:n.442C>T