Canonical Allele Identifier: CA1906411951
Gene: CXCL12 HGNC NCBI

Linked Data

dbSNP Id: rs1839821079

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.44386379G>C , CM000672.2:g.44386379G>C GRCh38
NC_000010.10:g.44881827G>C , CM000672.1:g.44881827G>C GRCh37
NC_000010.9:g.44201833G>C NCBI36
NG_016861.1:g.3719C>G
NG_016861.2:g.3719C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000496375.1:n.115C>G