Canonical Allele Identifier: CA2608932723
Gene: CXCL12 HGNC NCBI

Linked Data

dbSNP Id: rs2132058882

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.44386371G>A , CM000672.2:g.44386371G>A GRCh38
NC_000010.10:g.44881819G>A , CM000672.1:g.44881819G>A GRCh37
NC_000010.9:g.44201825G>A NCBI36
NG_016861.1:g.3727C>T
NG_016861.2:g.3727C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000496375.1:n.123C>T