Canonical Allele Identifier: CA1906411683
Gene: CXCL12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.44386080_44386081delinsCT , CM000672.2:g.44386080_44386081delinsCT GRCh38
NC_000010.10:g.44881528_44881529delinsCT , CM000672.1:g.44881528_44881529delinsCT GRCh37
NC_000010.9:g.44201534_44201535delinsCT NCBI36
NG_016861.1:g.4017_4018delinsAG
NG_016861.2:g.4017_4018delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000496375.1:n.413_414delinsAG