Canonical Allele Identifier: CA1268335638

Linked Data

dbSNP Id: rs1187367909

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88859366T>G , CM000664.2:g.88859366T>G GRCh38
NC_000002.11:g.89158879T>G , CM000664.1:g.89158879T>G GRCh37
NC_000002.10:g.88939994T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000377423.6:c.389-1683A>C (IGKV1-12) ENSP00000480537.2:n.389-1683A>C
ENST00000430694.5:c.37+1520A>C (IGKC) ENSP00000481923.2:n.37+1520A>C
ENST00000610638.3:c.398-1683A>C (IGKC) ENSP00000484499.3:n.398-1683A>C
ENST00000634828.1:c.383-1683A>C (IGKV1-8) ENSP00000489500.1:n.383-1683A>C