Canonical Allele Identifier: CA665410336

Gene: CXCL12

Linked Data

• dbSNP Id: rs17884027
• MyVariant Identifiers: chr10:g.44881443A>T (hg19) ; chr10:g.44385995A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.44385995A>T , CM000672.2:g.44385995A>T	GRCh38
NC_000010.10:g.44881443A>T , CM000672.1:g.44881443A>T	GRCh37
NC_000010.9:g.44201449A>T	NCBI36
NG_016861.1:g.4103T>A
NG_016861.2:g.4103T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496375.1:n.499T>A