Canonical Allele Identifier: CA2721597116
Gene: CXCL12 HGNC NCBI

Linked Data

dbSNP Id: rs1588908077
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.44386279T>G , CM000672.2:g.44386279T>G GRCh38
NC_000010.10:g.44881727T>G , CM000672.1:g.44881727T>G GRCh37
NC_000010.9:g.44201733T>G NCBI36
NG_016861.1:g.3819A>C
NG_016861.2:g.3819A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000496375.1:n.215A>C
Search 100 bp 5'
Search 100 bp 3'