Canonical Allele Identifier: CA2588653690

Gene: CXCL12

Linked Data

• dbSNP Id: rs2132033849
• gnomAD v3: 10-44370551-A-T
• gnomAD v4: 10-44370551-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.44370551A>T , CM000672.2:g.44370551A>T	GRCh38
NC_000010.10:g.44865999A>T , CM000672.1:g.44865999A>T	GRCh37
NC_000010.9:g.44186005A>T	NCBI36
NG_016861.1:g.19547T>A
NG_016861.2:g.19547T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374429.6:c.*2777T>A	ENSP00000363551.2:n.*2777T>A
NM_000609.6:c.*2777T>A	NP_000600.1:n.*2777T>A
NM_001277990.1:c.*2337T>A	NP_001264919.1:n.*2337T>A
XR_001747171.1:n.331+8086T>A
XR_001747172.1:n.331+8086T>A
XR_001747173.1:n.331+8086T>A
XR_001747174.1:n.331+8086T>A
NM_000609.7:c.*2777T>A	NP_000600.1:n.*2777T>A
NM_001277990.2:c.*2337T>A	NP_001264919.1:n.*2337T>A