Canonical Allele Identifier: CA1906411593
Gene: CXCL12 HGNC NCBI

Linked Data

dbSNP Id: rs1839808993
gnomAD v3: 10-44385970-C-CCTTA
gnomAD v4: 10-44385970-C-CCTTA
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.44385972_44385975dup , CM000672.2:g.44385972_44385975dup GRCh38
NC_000010.10:g.44881420_44881423dup , CM000672.1:g.44881420_44881423dup GRCh37
NC_000010.9:g.44201426_44201429dup NCBI36
NG_016861.1:g.4124_4127dup
NG_016861.2:g.4124_4127dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000496375.1:n.518+2_518+5dup
Search 100 bp 5'
Search 100 bp 3'