Canonical Allele Identifier: CA1268336273

Linked Data

dbSNP Id: rs1675133919

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88859805_88859806del , CM000664.2:g.88859805_88859806del GRCh38
NC_000002.11:g.89159317_89159318del , CM000664.1:g.89159317_89159318del GRCh37
NC_000002.10:g.88940432_88940433del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000377423.6:c.388+2080_388+2081del (IGKV1-12) ENSP00000480537.2:n.388+2080_388+2081del
ENST00000430694.5:c.37+1080_37+1081del (IGKC) ENSP00000481923.2:n.37+1080_37+1081del
ENST00000610638.3:c.397+1719_397+1720del (IGKC) ENSP00000484499.3:n.397+1719_397+1720del
ENST00000634828.1:c.382+1719_382+1720del (IGKV1-8) ENSP00000489500.1:n.382+1719_382+1720del