Canonical Allele Identifier: CA665410530
Gene: CXCL12 HGNC NCBI

Linked Data

dbSNP Id: rs1312357829
MyVariant Identifiers: chr10:g.44881804G>C (hg19) chr10:g.44386356G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.44386356G>C , CM000672.2:g.44386356G>C GRCh38
NC_000010.10:g.44881804G>C , CM000672.1:g.44881804G>C GRCh37
NC_000010.9:g.44201810G>C NCBI36
NG_016861.1:g.3742C>G
NG_016861.2:g.3742C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000496375.1:n.138C>G
Search 100 bp 5'
Search 100 bp 3'