Canonical Allele Identifier: CA646854900

Linked Data

dbSNP Id: rs1675133842
gnomAD v3: 2-88859805-G-A
gnomAD v4: 2-88859805-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88859805G>A , CM000664.2:g.88859805G>A GRCh38
NC_000002.11:g.89159317G>A , CM000664.1:g.89159317G>A GRCh37
NC_000002.10:g.88940432G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000377423.6:c.388+2081C>T (IGKV1-12) ENSP00000480537.2:n.388+2081C>T
ENST00000430694.5:c.37+1081C>T (IGKC) ENSP00000481923.2:n.37+1081C>T
ENST00000610638.3:c.397+1720C>T (IGKC) ENSP00000484499.3:n.397+1720C>T
ENST00000634828.1:c.382+1720C>T (IGKV1-8) ENSP00000489500.1:n.382+1720C>T