Canonical Allele Identifier: CA1033367380

Linked Data

dbSNP Id: rs1675134153

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88859807del , CM000664.2:g.88859807del GRCh38
NC_000002.11:g.89159319del , CM000664.1:g.89159319del GRCh37
NC_000002.10:g.88940434del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000377423.6:c.388+2079del (IGKV1-12) ENSP00000480537.2:n.388+2079del
ENST00000430694.5:c.37+1079del (IGKC) ENSP00000481923.2:n.37+1079del
ENST00000610638.3:c.397+1718del (IGKC) ENSP00000484499.3:n.397+1718del
ENST00000634828.1:c.382+1718del (IGKV1-8) ENSP00000489500.1:n.382+1718del