Canonical Allele Identifier: CA206329601
Gene: CXCL12 HGNC NCBI

Linked Data

dbSNP Id: rs531498594
gnomAD v3: 10-44386113-C-T
gnomAD v4: 10-44386113-C-T
MyVariant Identifiers: chr10:g.44881561C>T (hg19) chr10:g.44386113C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.44386113C>T , CM000672.2:g.44386113C>T GRCh38
NC_000010.10:g.44881561C>T , CM000672.1:g.44881561C>T GRCh37
NC_000010.9:g.44201567C>T NCBI36
NG_016861.1:g.3985G>A
NG_016861.2:g.3985G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000496375.1:n.381G>A
Search 100 bp 5'
Search 100 bp 3'