Canonical Allele Identifier: CA206317105

Gene: CXCL12

Linked Data

• dbSNP Id: rs113379535
• gnomAD v2: 10-44865966-C-T
• gnomAD v3: 10-44370518-C-T
• gnomAD v4: 10-44370518-C-T
• MyVariant Identifiers: chr10:g.44865966C>T (hg19) ; chr10:g.44370518C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.44370518C>T , CM000672.2:g.44370518C>T	GRCh38
NC_000010.10:g.44865966C>T , CM000672.1:g.44865966C>T	GRCh37
NC_000010.9:g.44185972C>T	NCBI36
NG_016861.1:g.19580G>A
NG_016861.2:g.19580G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374429.6:c.*2810G>A	ENSP00000363551.2:n.*2810G>A
NM_000609.6:c.*2810G>A	NP_000600.1:n.*2810G>A
NM_001277990.1:c.*2370G>A	NP_001264919.1:n.*2370G>A
XR_001747171.1:n.331+8119G>A
XR_001747172.1:n.331+8119G>A
XR_001747173.1:n.331+8119G>A
XR_001747174.1:n.331+8119G>A
NM_000609.7:c.*2810G>A	NP_000600.1:n.*2810G>A
NM_001277990.2:c.*2370G>A	NP_001264919.1:n.*2370G>A