Canonical Allele Identifier: CA206317059

Gene: CXCL12

Linked Data

• dbSNP Id: rs766555469
• gnomAD v2: 10-44865858-TGA-T
• gnomAD v3: 10-44370410-TGA-T
• gnomAD v4: 10-44370410-TGA-T
• MyVariant Identifiers: chr10:g.44865859_44865860del (hg19) ; chr10:g.44370411_44370412del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.44370414_44370415del , CM000672.2:g.44370414_44370415del	GRCh38
NC_000010.10:g.44865862_44865863del , CM000672.1:g.44865862_44865863del	GRCh37
NC_000010.9:g.44185868_44185869del	NCBI36
NG_016861.1:g.19686_19687del
NG_016861.2:g.19686_19687del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374429.6:c.*2916_*2917del	ENSP00000363551.2:n.*2916_*2917del
NM_000609.6:c.*2916_*2917del	NP_000600.1:n.*2916_*2917del
NM_001277990.1:c.*2476_*2477del	NP_001264919.1:n.*2476_*2477del
XR_001747171.1:n.331+8225_331+8226del
XR_001747172.1:n.331+8225_331+8226del
XR_001747173.1:n.331+8225_331+8226del
XR_001747174.1:n.331+8225_331+8226del
NM_000609.7:c.*2916_*2917del	NP_000600.1:n.*2916_*2917del
NM_001277990.2:c.*2476_*2477del	NP_001264919.1:n.*2476_*2477del