Canonical Allele Identifier: CA646854854

Linked Data

dbSNP Id: rs1675131870
gnomAD v3: 2-88859796-A-G
gnomAD v4: 2-88859796-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88859796A>G , CM000664.2:g.88859796A>G GRCh38
NC_000002.11:g.89159308A>G , CM000664.1:g.89159308A>G GRCh37
NC_000002.10:g.88940423A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000377423.6:c.388+2090T>C (IGKV1-12) ENSP00000480537.2:n.388+2090T>C
ENST00000430694.5:c.37+1090T>C (IGKC) ENSP00000481923.2:n.37+1090T>C
ENST00000610638.3:c.397+1729T>C (IGKC) ENSP00000484499.3:n.397+1729T>C
ENST00000634828.1:c.382+1729T>C (IGKV1-8) ENSP00000489500.1:n.382+1729T>C