Canonical Allele Identifier: CA2608929335

Gene: CXCL12

Linked Data

• gnomAD v4: 10-44372814-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.44372814C>A , CM000672.2:g.44372814C>A	GRCh38
NC_000010.10:g.44868262C>A , CM000672.1:g.44868262C>A	GRCh37
NC_000010.9:g.44188268C>A	NCBI36
NG_016861.1:g.17284G>T
NG_016861.2:g.17284G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000374429.6:c.*514G>T	ENSP00000363551.2:n.*514G>T
ENST00000395793.7:c.*74G>T	ENSP00000379139.3:n.*74G>T
NM_000609.6:c.*514G>T	NP_000600.1:n.*514G>T
NM_001277990.1:c.*74G>T	NP_001264919.1:n.*74G>T
XR_001747171.1:n.331+5823G>T
XR_001747172.1:n.331+5823G>T
XR_001747173.1:n.331+5823G>T
XR_001747174.1:n.331+5823G>T
NM_000609.7:c.*514G>T	NP_000600.1:n.*514G>T
NM_001277990.2:c.*74G>T	NP_001264919.1:n.*74G>T