Canonical Allele Identifier: CA1268336271

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88859804G= , CM000664.2:g.88859804G= GRCh38
NC_000002.11:g.89159316G= , CM000664.1:g.89159316G= GRCh37
NC_000002.10:g.88940431G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000377423.6:c.388+2082C= (IGKV1-12) ENSP00000480537.2:n.388+2082C=
ENST00000430694.5:c.37+1082C= (IGKC) ENSP00000481923.2:n.37+1082C=
ENST00000610638.3:c.397+1721C= (IGKC) ENSP00000484499.3:n.397+1721C=
ENST00000634828.1:c.382+1721C= (IGKV1-8) ENSP00000489500.1:n.382+1721C=