Canonical Allele Identifier: CA927778578
Gene: CXCL12 HGNC NCBI

Linked Data

dbSNP Id: rs1839822207
gnomAD v3: 10-44386453-T-C
gnomAD v4: 10-44386453-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.44386453T>C , CM000672.2:g.44386453T>C GRCh38
NC_000010.10:g.44881901T>C , CM000672.1:g.44881901T>C GRCh37
NC_000010.9:g.44201907T>C NCBI36
NG_016861.1:g.3645A>G
NG_016861.2:g.3645A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000496375.1:n.41A>G
Search 100 bp 5'
Search 100 bp 3'