Canonical Allele Identifier: CA542414943
Gene:

Linked Data

dbSNP Id: rs1193032113
gnomAD v2: 3-34962850-C-T
gnomAD v3: 3-34921358-C-T
gnomAD v4: 3-34921358-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.34921358C>T , CM000665.2:g.34921358C>T GRCh38
NC_000003.11:g.34962850C>T , CM000665.1:g.34962850C>T GRCh37
NC_000003.10:g.34937854C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110817.1:n.207-41892G>A