Canonical Allele Identifier: CA1268336040

Linked Data

dbSNP Id: rs1675120082

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88859624del , CM000664.2:g.88859624del GRCh38
NC_000002.11:g.89159136del , CM000664.1:g.89159136del GRCh37
NC_000002.10:g.88940251del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000377423.6:c.389-1941del (IGKV1-12) ENSP00000480537.2:n.389-1941del
ENST00000430694.5:c.37+1262del (IGKC) ENSP00000481923.2:n.37+1262del
ENST00000610638.3:c.397+1901del (IGKC) ENSP00000484499.3:n.397+1901del
ENST00000634828.1:c.382+1901del (IGKV1-8) ENSP00000489500.1:n.382+1901del