Canonical Allele Identifier: CA1048602132
Gene:

Linked Data

dbSNP Id: rs2041753958
gnomAD v3: 3-61428237-A-T
gnomAD v4: 3-61428237-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.61428237A>T , CM000665.2:g.61428237A>T GRCh38
NC_000003.11:g.61413911A>T , CM000665.1:g.61413911A>T GRCh37
NC_000003.10:g.61388951A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940892.1:n.164+277T>A
XR_940893.1:n.164+277T>A
XR_001740725.1:n.202+277T>A
XR_940892.2:n.202+277T>A