Canonical Allele Identifier: CA206329581
Gene: CXCL12 HGNC NCBI

Linked Data

dbSNP Id: rs1013364019
gnomAD v4: 10-44386059-G-T
MyVariant Identifiers: chr10:g.44386059G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.44386059G>T , CM000672.2:g.44386059G>T GRCh38
NC_000010.10:g.44881507G>T , CM000672.1:g.44881507G>T GRCh37
NC_000010.9:g.44201513G>T NCBI36
NG_016861.1:g.4039C>A
NG_016861.2:g.4039C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000496375.1:n.435C>A
Search 100 bp 5'
Search 100 bp 3'