Canonical Allele Identifier: CA1630848231
Gene: CXCL12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.44372809C= , CM000672.2:g.44372809C= GRCh38
NC_000010.10:g.44868257C= , CM000672.1:g.44868257C= GRCh37
NC_000010.9:g.44188263C= NCBI36
NG_016861.1:g.17289G=
NG_016861.2:g.17289G=

Transcript Alleles

HGVS Amino-acid change
ENST00000374429.6:c.*519G= ENSP00000363551.2:n.*519G=
ENST00000395793.7:c.*79G= ENSP00000379139.3:n.*79G=
NM_000609.6:c.*519G= NP_000600.1:n.*519G=
NM_001277990.1:c.*79G= NP_001264919.1:n.*79G=
XR_001747171.1:n.331+5828G=
XR_001747172.1:n.331+5828G=
XR_001747173.1:n.331+5828G=
XR_001747174.1:n.331+5828G=
NM_000609.7:c.*519G= NP_000600.1:n.*519G=
NM_001277990.2:c.*79G= NP_001264919.1:n.*79G=