Canonical Allele Identifier: CA2608932759
Gene: CXCL12 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.44386401G>C , CM000672.2:g.44386401G>C GRCh38
NC_000010.10:g.44881849G>C , CM000672.1:g.44881849G>C GRCh37
NC_000010.9:g.44201855G>C NCBI36
NG_016861.1:g.3697C>G
NG_016861.2:g.3697C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000496375.1:n.93C>G