Canonical Allele Identifier: CA665400673

Gene: CXCL12

Linked Data

• dbSNP Id: rs1478115792
• gnomAD v3: 10-44370362-A-C
• gnomAD v4: 10-44370362-A-C
• MyVariant Identifiers: chr10:g.44865810A>C (hg19) ; chr10:g.44370362A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.44370362A>C , CM000672.2:g.44370362A>C	GRCh38
NC_000010.10:g.44865810A>C , CM000672.1:g.44865810A>C	GRCh37
NC_000010.9:g.44185816A>C	NCBI36
NG_016861.1:g.19736T>G
NG_016861.2:g.19736T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374429.6:c.*2966T>G	ENSP00000363551.2:n.*2966T>G
NM_000609.6:c.*2966T>G	NP_000600.1:n.*2966T>G
NM_001277990.1:c.*2526T>G	NP_001264919.1:n.*2526T>G
XR_001747171.1:n.331+8275T>G
XR_001747172.1:n.331+8275T>G
XR_001747173.1:n.331+8275T>G
XR_001747174.1:n.331+8275T>G
NM_000609.7:c.*2966T>G	NP_000600.1:n.*2966T>G
NM_001277990.2:c.*2526T>G	NP_001264919.1:n.*2526T>G