Canonical Allele Identifier: CA1268336079

Linked Data

dbSNP Id: rs556771940

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88859655C>A , CM000664.2:g.88859655C>A GRCh38
NC_000002.11:g.89159167C>A , CM000664.1:g.89159167C>A GRCh37
NC_000002.10:g.88940282C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000377423.6:c.389-1972G>T (IGKV1-12) ENSP00000480537.2:n.389-1972G>T
ENST00000430694.5:c.37+1231G>T (IGKC) ENSP00000481923.2:n.37+1231G>T
ENST00000610638.3:c.397+1870G>T (IGKC) ENSP00000484499.3:n.397+1870G>T
ENST00000634828.1:c.382+1870G>T (IGKV1-8) ENSP00000489500.1:n.382+1870G>T