Canonical Allele Identifier: CA2608932705
Gene: CXCL12 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.44386356G>A , CM000672.2:g.44386356G>A GRCh38
NC_000010.10:g.44881804G>A , CM000672.1:g.44881804G>A GRCh37
NC_000010.9:g.44201810G>A NCBI36
NG_016861.1:g.3742C>T
NG_016861.2:g.3742C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000496375.1:n.138C>T