Canonical Allele Identifier: CA1268335769

Linked Data

dbSNP Id: rs1675097590
gnomAD v3: 2-88859444-T-C
gnomAD v4: 2-88859444-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88859444T>C , CM000664.2:g.88859444T>C GRCh38
NC_000002.11:g.89158956T>C , CM000664.1:g.89158956T>C GRCh37
NC_000002.10:g.88940071T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000377423.6:c.389-1761A>G (IGKV1-12) ENSP00000480537.2:n.389-1761A>G
ENST00000430694.5:c.37+1442A>G (IGKC) ENSP00000481923.2:n.37+1442A>G
ENST00000610638.3:c.398-1761A>G (IGKC) ENSP00000484499.3:n.398-1761A>G
ENST00000634828.1:c.383-1761A>G (IGKV1-8) ENSP00000489500.1:n.383-1761A>G