Canonical Allele Identifier: CA592922676
Gene: CXCL12 HGNC NCBI

Linked Data

dbSNP Id: rs1564466694
gnomAD v2: 10-44881769-G-GCCCTGGGGACACGTCCCTGT
gnomAD v3: 10-44386321-G-GCCCTGGGGACACGTCCCTGT
gnomAD v4: 10-44386321-G-GCCCTGGGGACACGTCCCTGT
MyVariant Identifiers: chr10:g.44881769_44881770insCCCTGGGGACACGTCCCTGT (hg19) chr10:g.44386321_44386322insCCCTGGGGACACGTCCCTGT (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.44386331_44386350dup , CM000672.2:g.44386331_44386350dup GRCh38
NC_000010.10:g.44881779_44881798dup , CM000672.1:g.44881779_44881798dup GRCh37
NC_000010.9:g.44201785_44201804dup NCBI36
NG_016861.1:g.3757_3776dup
NG_016861.2:g.3757_3776dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000496375.1:n.153_172dup
Search 100 bp 5'
Search 100 bp 3'