Canonical Allele Identifier: CA1268336308

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88859827T= , CM000664.2:g.88859827T= GRCh38
NC_000002.11:g.89159339T= , CM000664.1:g.89159339T= GRCh37
NC_000002.10:g.88940454T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000377423.6:c.388+2059A= (IGKV1-12) ENSP00000480537.2:n.388+2059A=
ENST00000430694.5:c.37+1059A= (IGKC) ENSP00000481923.2:n.37+1059A=
ENST00000610638.3:c.397+1698A= (IGKC) ENSP00000484499.3:n.397+1698A=
ENST00000634828.1:c.382+1698A= (IGKV1-8) ENSP00000489500.1:n.382+1698A=