Canonical Allele Identifier: CA1906411917
Gene: CXCL12 HGNC NCBI

Linked Data

dbSNP Id: rs1839818840
gnomAD v3: 10-44386347-G-A
gnomAD v4: 10-44386347-G-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.44386347G>A , CM000672.2:g.44386347G>A GRCh38
NC_000010.10:g.44881795G>A , CM000672.1:g.44881795G>A GRCh37
NC_000010.9:g.44201801G>A NCBI36
NG_016861.1:g.3751C>T
NG_016861.2:g.3751C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000496375.1:n.147C>T
Search 100 bp 5'
Search 100 bp 3'