Canonical Allele Identifier: CA927778514
Gene: CXCL12 HGNC NCBI

Linked Data

dbSNP Id: rs1839817054
gnomAD v3: 10-44386257-C-T
gnomAD v4: 10-44386257-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.44386257C>T , CM000672.2:g.44386257C>T GRCh38
NC_000010.10:g.44881705C>T , CM000672.1:g.44881705C>T GRCh37
NC_000010.9:g.44201711C>T NCBI36
NG_016861.1:g.3841G>A
NG_016861.2:g.3841G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000496375.1:n.237G>A
Search 100 bp 5'
Search 100 bp 3'