Canonical Allele Identifier: CA1906433337
Gene: CXCL12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.44370367G= , CM000672.2:g.44370367G= GRCh38
NC_000010.10:g.44865815G= , CM000672.1:g.44865815G= GRCh37
NC_000010.9:g.44185821G= NCBI36
NG_016861.1:g.19731C=
NG_016861.2:g.19731C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374429.6:c.*2961C= ENSP00000363551.2:n.*2961C=
NM_000609.6:c.*2961C= NP_000600.1:n.*2961C=
NM_001277990.1:c.*2521C= NP_001264919.1:n.*2521C=
XR_001747171.1:n.331+8270C=
XR_001747172.1:n.331+8270C=
XR_001747173.1:n.331+8270C=
XR_001747174.1:n.331+8270C=
NM_000609.7:c.*2961C= NP_000600.1:n.*2961C=
NM_001277990.2:c.*2521C= NP_001264919.1:n.*2521C=