Canonical Allele Identifier: CA1033367264

Linked Data

dbSNP Id: rs1675130897

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88859784_88859785insCT , CM000664.2:g.88859784_88859785insCT GRCh38
NC_000002.11:g.89159296_89159297insCT , CM000664.1:g.89159296_89159297insCT GRCh37
NC_000002.10:g.88940411_88940412insCT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000377423.6:c.389-2101_389-2100insGA (IGKV1-12) ENSP00000480537.2:n.389-2101_389-2100insGA
ENST00000430694.5:c.37+1102_37+1103insGA (IGKC) ENSP00000481923.2:n.37+1102_37+1103insGA
ENST00000610638.3:c.397+1741_397+1742insGA (IGKC) ENSP00000484499.3:n.397+1741_397+1742insGA
ENST00000634828.1:c.382+1741_382+1742insGA (IGKV1-8) ENSP00000489500.1:n.382+1741_382+1742insGA