Canonical Allele Identifier: CA1906411693
Gene: CXCL12 HGNC NCBI

Linked Data

dbSNP Id: rs1839812596
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.44386087C>A , CM000672.2:g.44386087C>A GRCh38
NC_000010.10:g.44881535C>A , CM000672.1:g.44881535C>A GRCh37
NC_000010.9:g.44201541C>A NCBI36
NG_016861.1:g.4011G>T
NG_016861.2:g.4011G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000496375.1:n.407G>T
Search 100 bp 5'
Search 100 bp 3'