Canonical Allele Identifier: CA119898

Gene: CXCL12

Linked Data

• ClinVar Variation Id: 8762
• ClinVar RCV Id: RCV000009307
• dbSNP Id: rs387906400
• gnomAD v4: 10-44378102-C-T
• MyVariant Identifiers: chr10:g.44873550C>T (hg19) ; chr10:g.44378102C>T (hg38)
• PubMed: PMID:9430590

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.44378102C>T , CM000672.2:g.44378102C>T	GRCh38
NC_000010.10:g.44873550C>T , CM000672.1:g.44873550C>T	GRCh37
NC_000010.9:g.44193556C>T	NCBI36
NG_016861.1:g.11996G>A
NG_016861.2:g.11996G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343575.11:c.*531G>A MANE Select	ENSP00000339913.6:n.*531G>A
ENST00000343575.10:c.*531G>A	ENSP00000339913.6:n.*531G>A
ENST00000374426.6:c.266+535G>A	ENSP00000363548.2:n.266+535G>A
ENST00000374429.6:c.266+535G>A	ENSP00000363551.2:n.266+535G>A
ENST00000395793.7:c.109+2731G>A	ENSP00000379139.3:n.109+2731G>A
ENST00000395794.2:c.267-197G>A	ENSP00000379140.2:n.267-197G>A
ENST00000395795.5:c.110+2730G>A	ENSP00000379141.5:n.110+2730G>A
NM_000609.6:c.266+535G>A	NP_000600.1:n.266+535G>A
NM_001033886.2:c.266+535G>A	NP_001029058.1:n.266+535G>A
NM_001178134.1:c.267-197G>A	NP_001171605.1:n.267-197G>A
NM_001277990.1:c.109+2731G>A	NP_001264919.1:n.109+2731G>A
NM_199168.3:c.*531G>A	NP_954637.1:n.*531G>A
XR_001747171.1:n.331+535G>A
XR_001747172.1:n.331+535G>A
XR_001747173.1:n.331+535G>A
XR_001747174.1:n.331+535G>A
NM_000609.7:c.266+535G>A	NP_000600.1:n.266+535G>A
NM_001178134.2:c.267-197G>A	NP_001171605.1:n.267-197G>A
NM_001277990.2:c.109+2731G>A	NP_001264919.1:n.109+2731G>A
NM_199168.4:c.*531G>A MANE Select	NP_954637.1:n.*531G>A