Canonical Allele Identifier: CA2608932578
Gene: CXCL12 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.44386227T>G , CM000672.2:g.44386227T>G GRCh38
NC_000010.10:g.44881675T>G , CM000672.1:g.44881675T>G GRCh37
NC_000010.9:g.44201681T>G NCBI36
NG_016861.1:g.3871A>C
NG_016861.2:g.3871A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000496375.1:n.267A>C