Canonical Allele Identifier: CA2608932573
Gene: CXCL12 HGNC NCBI

Linked Data

dbSNP Id: rs2132058708

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.44386224G>A , CM000672.2:g.44386224G>A GRCh38
NC_000010.10:g.44881672G>A , CM000672.1:g.44881672G>A GRCh37
NC_000010.9:g.44201678G>A NCBI36
NG_016861.1:g.3874C>T
NG_016861.2:g.3874C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000496375.1:n.270C>T