Canonical Allele Identifier: CA1033396046

Linked Data

gnomAD v3: 2-88859477-G-T
gnomAD v4: 2-88859477-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88859477G>T , CM000664.2:g.88859477G>T GRCh38
NC_000002.11:g.89158989G>T , CM000664.1:g.89158989G>T GRCh37
NC_000002.10:g.88940104G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000377423.6:c.389-1794C>A (IGKV1-12) ENSP00000480537.2:n.389-1794C>A
ENST00000430694.5:c.37+1409C>A (IGKC) ENSP00000481923.2:n.37+1409C>A
ENST00000610638.3:c.398-1794C>A (IGKC) ENSP00000484499.3:n.398-1794C>A
ENST00000634828.1:c.383-1794C>A (IGKV1-8) ENSP00000489500.1:n.383-1794C>A