Canonical Allele Identifier: CA206329596
Gene: CXCL12 HGNC NCBI

Linked Data

dbSNP Id: rs939705623
gnomAD v3: 10-44386111-A-G
gnomAD v4: 10-44386111-A-G
MyVariant Identifiers: chr10:g.44881559A>G (hg19) chr10:g.44386111A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.44386111A>G , CM000672.2:g.44386111A>G GRCh38
NC_000010.10:g.44881559A>G , CM000672.1:g.44881559A>G GRCh37
NC_000010.9:g.44201565A>G NCBI36
NG_016861.1:g.3987T>C
NG_016861.2:g.3987T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000496375.1:n.383T>C
Search 100 bp 5'
Search 100 bp 3'