Canonical Allele Identifier: CA1268335979

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88859585G= , CM000664.2:g.88859585G= GRCh38
NC_000002.11:g.89159097G= , CM000664.1:g.89159097G= GRCh37
NC_000002.10:g.88940212G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000377423.6:c.389-1902C= (IGKV1-12) ENSP00000480537.2:n.389-1902C=
ENST00000430694.5:c.37+1301C= (IGKC) ENSP00000481923.2:n.37+1301C=
ENST00000610638.3:c.398-1902C= (IGKC) ENSP00000484499.3:n.398-1902C=
ENST00000634828.1:c.383-1902C= (IGKV1-8) ENSP00000489500.1:n.383-1902C=