Canonical Allele Identifier: CA665410532
Gene: CXCL12 HGNC NCBI

Linked Data

dbSNP Id: rs1413125586
MyVariant Identifiers: chr10:g.44881805G>A (hg19) chr10:g.44386357G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.44386357G>A , CM000672.2:g.44386357G>A GRCh38
NC_000010.10:g.44881805G>A , CM000672.1:g.44881805G>A GRCh37
NC_000010.9:g.44201811G>A NCBI36
NG_016861.1:g.3741C>T
NG_016861.2:g.3741C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000496375.1:n.137C>T
Search 100 bp 5'
Search 100 bp 3'