Canonical Allele Identifier: CA927778553
Gene: CXCL12 HGNC NCBI

Linked Data

dbSNP Id: rs1789520932
gnomAD v3: 10-44386351-G-GTCCT
gnomAD v4: 10-44386351-G-GTCCT
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.44386352_44386355dup , CM000672.2:g.44386352_44386355dup GRCh38
NC_000010.10:g.44881800_44881803dup , CM000672.1:g.44881800_44881803dup GRCh37
NC_000010.9:g.44201806_44201809dup NCBI36
NG_016861.1:g.3743_3746dup
NG_016861.2:g.3743_3746dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000496375.1:n.139_142dup
Search 100 bp 5'
Search 100 bp 3'