Canonical Allele Identifier: CA13189019
Gene: CXCL12 HGNC NCBI
MyVariant.info:
GRCh38 chr10:g.44386212C>T
GRCh37 chr10:g.44881660C>T
gnomAD v2:
10:44881660 C / T
gnomAD v3:
10:44386212 C / T
gnomAD v4:
chr10-44386212-C-T
Joint Max Group AF 0.30153091 (NFE)
Genomes Max Group AF 0.30145646 (NFE)
Exomes Max Group AF 0.26360133 (NFE)
dbSNP:
17885289
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.44386212C>T , CM000672.2:g.44386212C>T GRCh38
NC_000010.10:g.44881660C>T , CM000672.1:g.44881660C>T GRCh37
NC_000010.9:g.44201666C>T NCBI36
NG_016861.1:g.3886G>A
NG_016861.2:g.3886G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000496375.1:n.282G>A
Search 100 bp 5'
Search 100 bp 3'