Canonical Allele Identifier: CA2608932618
Gene: CXCL12 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.44386265T>C , CM000672.2:g.44386265T>C GRCh38
NC_000010.10:g.44881713T>C , CM000672.1:g.44881713T>C GRCh37
NC_000010.9:g.44201719T>C NCBI36
NG_016861.1:g.3833A>G
NG_016861.2:g.3833A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000496375.1:n.229A>G