Canonical Allele Identifier: CA1906401624
Gene: CXCL12 HGNC NCBI

Linked Data

dbSNP Id: rs1839347502
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.44372818T>C , CM000672.2:g.44372818T>C GRCh38
NC_000010.10:g.44868266T>C , CM000672.1:g.44868266T>C GRCh37
NC_000010.9:g.44188272T>C NCBI36
NG_016861.1:g.17280A>G
NG_016861.2:g.17280A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000374429.6:c.*510A>G ENSP00000363551.2:n.*510A>G
ENST00000395793.7:c.*70A>G ENSP00000379139.3:n.*70A>G
NM_000609.6:c.*510A>G NP_000600.1:n.*510A>G
NM_001277990.1:c.*70A>G NP_001264919.1:n.*70A>G
XR_001747171.1:n.331+5819A>G
XR_001747172.1:n.331+5819A>G
XR_001747173.1:n.331+5819A>G
XR_001747174.1:n.331+5819A>G
NM_000609.7:c.*510A>G NP_000600.1:n.*510A>G
NM_001277990.2:c.*70A>G NP_001264919.1:n.*70A>G
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