Canonical Allele Identifier: CA1268335641

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88859368T= , CM000664.2:g.88859368T= GRCh38
NC_000002.11:g.89158881T= , CM000664.1:g.89158881T= GRCh37
NC_000002.10:g.88939996T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000377423.6:c.389-1685A= (IGKV1-12) ENSP00000480537.2:n.389-1685A=
ENST00000430694.5:c.37+1518A= (IGKC) ENSP00000481923.2:n.37+1518A=
ENST00000610638.3:c.398-1685A= (IGKC) ENSP00000484499.3:n.398-1685A=
ENST00000634828.1:c.383-1685A= (IGKV1-8) ENSP00000489500.1:n.383-1685A=