Canonical Allele Identifier: CA1906401623
Gene: CXCL12 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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