Canonical Allele Identifier: CA1906411651
Gene: CXCL12 HGNC NCBI

Linked Data

dbSNP Id: rs1839811294

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.44386028T>A , CM000672.2:g.44386028T>A GRCh38
NC_000010.10:g.44881476T>A , CM000672.1:g.44881476T>A GRCh37
NC_000010.9:g.44201482T>A NCBI36
NG_016861.1:g.4070A>T
NG_016861.2:g.4070A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000496375.1:n.466A>T