Canonical Allele Identifier: CA2608932795
Gene: CXCL12 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.44386443A>G , CM000672.2:g.44386443A>G GRCh38
NC_000010.10:g.44881891A>G , CM000672.1:g.44881891A>G GRCh37
NC_000010.9:g.44201897A>G NCBI36
NG_016861.1:g.3655T>C
NG_016861.2:g.3655T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000496375.1:n.51T>C