Canonical Allele Identifier: CA206329672
Gene: CXCL12 HGNC NCBI

Linked Data

dbSNP Id: rs907185751
gnomAD v2: 10-44881740-G-A
gnomAD v3: 10-44386292-G-A
gnomAD v4: 10-44386292-G-A
MyVariant Identifiers: chr10:g.44881740G>A (hg19) chr10:g.44386292G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.44386292G>A , CM000672.2:g.44386292G>A GRCh38
NC_000010.10:g.44881740G>A , CM000672.1:g.44881740G>A GRCh37
NC_000010.9:g.44201746G>A NCBI36
NG_016861.1:g.3806C>T
NG_016861.2:g.3806C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000496375.1:n.202C>T
Search 100 bp 5'
Search 100 bp 3'