Canonical Allele Identifier: CA1906411944
Gene: CXCL12 HGNC NCBI

Linked Data

dbSNP Id: rs987052224

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.44386370G>T , CM000672.2:g.44386370G>T GRCh38
NC_000010.10:g.44881818G>T , CM000672.1:g.44881818G>T GRCh37
NC_000010.9:g.44201824G>T NCBI36
NG_016861.1:g.3728C>A
NG_016861.2:g.3728C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000496375.1:n.124C>A