Canonical Allele Identifier: CA534266664

Linked Data

dbSNP Id: rs6547795
gnomAD v2: 2-89159180-C-A
gnomAD v3: 2-88859668-C-A
gnomAD v4: 2-88859668-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88859668C>A , CM000664.2:g.88859668C>A GRCh38
NC_000002.11:g.89159180C>A , CM000664.1:g.89159180C>A GRCh37
NC_000002.10:g.88940295C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000377423.6:c.389-1985G>T (IGKV1-12) ENSP00000480537.2:n.389-1985G>T
ENST00000430694.5:c.37+1218G>T (IGKC) ENSP00000481923.2:n.37+1218G>T
ENST00000610638.3:c.397+1857G>T (IGKC) ENSP00000484499.3:n.397+1857G>T
ENST00000634828.1:c.382+1857G>T (IGKV1-8) ENSP00000489500.1:n.382+1857G>T