Canonical Allele Identifier: CA76316062
Gene:

Linked Data

dbSNP Id: rs1022615135
gnomAD v3: 3-61428164-C-T
gnomAD v4: 3-61428164-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.61428164C>T , CM000665.2:g.61428164C>T GRCh38
NC_000003.11:g.61413838C>T , CM000665.1:g.61413838C>T GRCh37
NC_000003.10:g.61388878C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_940892.1:n.164+350G>A
XR_940893.1:n.164+350G>A
XR_001740725.1:n.202+350G>A
XR_940892.2:n.202+350G>A