Canonical Allele Identifier: CA1268336289

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88859814A= , CM000664.2:g.88859814A= GRCh38
NC_000002.11:g.89159326A= , CM000664.1:g.89159326A= GRCh37
NC_000002.10:g.88940441A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000377423.6:c.388+2072T= (IGKV1-12) ENSP00000480537.2:n.388+2072T=
ENST00000430694.5:c.37+1072T= (IGKC) ENSP00000481923.2:n.37+1072T=
ENST00000610638.3:c.397+1711T= (IGKC) ENSP00000484499.3:n.397+1711T=
ENST00000634828.1:c.382+1711T= (IGKV1-8) ENSP00000489500.1:n.382+1711T=