Canonical Allele Identifier: CA894282011

Linked Data

dbSNP Id: rs530954009

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88859703G>C , CM000664.2:g.88859703G>C GRCh38
NC_000002.11:g.89159215G>C , CM000664.1:g.89159215G>C GRCh37
NC_000002.10:g.88940330G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000377423.6:c.389-2020C>G (IGKV1-12) ENSP00000480537.2:n.389-2020C>G
ENST00000430694.5:c.37+1183C>G (IGKC) ENSP00000481923.2:n.37+1183C>G
ENST00000610638.3:c.397+1822C>G (IGKC) ENSP00000484499.3:n.397+1822C>G
ENST00000634828.1:c.382+1822C>G (IGKV1-8) ENSP00000489500.1:n.382+1822C>G