Canonical Allele Identifier: CA1906411734
Gene: CXCL12 HGNC NCBI

Linked Data

dbSNP Id: rs1026156869
gnomAD v4: 10-44386118-C-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.44386118C>G , CM000672.2:g.44386118C>G GRCh38
NC_000010.10:g.44881566C>G , CM000672.1:g.44881566C>G GRCh37
NC_000010.9:g.44201572C>G NCBI36
NG_016861.1:g.3980G>C
NG_016861.2:g.3980G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000496375.1:n.376G>C
Search 100 bp 5'
Search 100 bp 3'