Canonical Allele Identifier: CA665410371
Gene: CXCL12 HGNC NCBI

Linked Data

dbSNP Id: rs1316683550
MyVariant Identifiers: chr10:g.44881522del (hg19) chr10:g.44386074del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.44386077del , CM000672.2:g.44386077del GRCh38
NC_000010.10:g.44881525del , CM000672.1:g.44881525del GRCh37
NC_000010.9:g.44201531del NCBI36
NG_016861.1:g.4024del
NG_016861.2:g.4024del

Transcript Alleles

HGVS Amino-acid Change
ENST00000496375.1:n.420del
Search 100 bp 5'
Search 100 bp 3'