Canonical Allele Identifier: CA2608926732

Gene: CXCL12

Linked Data

• gnomAD v4: 10-44370457-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.44370457A>G , CM000672.2:g.44370457A>G	GRCh38
NC_000010.10:g.44865905A>G , CM000672.1:g.44865905A>G	GRCh37
NC_000010.9:g.44185911A>G	NCBI36
NG_016861.1:g.19641T>C
NG_016861.2:g.19641T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000374429.6:c.*2871T>C	ENSP00000363551.2:n.*2871T>C
NM_000609.6:c.*2871T>C	NP_000600.1:n.*2871T>C
NM_001277990.1:c.*2431T>C	NP_001264919.1:n.*2431T>C
XR_001747171.1:n.331+8180T>C
XR_001747172.1:n.331+8180T>C
XR_001747173.1:n.331+8180T>C
XR_001747174.1:n.331+8180T>C
NM_000609.7:c.*2871T>C	NP_000600.1:n.*2871T>C
NM_001277990.2:c.*2431T>C	NP_001264919.1:n.*2431T>C