Canonical Allele Identifier: CA11143968
Gene:

Linked Data

dbSNP Id: rs13403149
gnomAD v2: 2-2843308-G-A
gnomAD v3: 2-2839536-G-A
gnomAD v4: 2-2839536-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.2839536G>A , CM000664.2:g.2839536G>A GRCh38
NC_000002.11:g.2843308G>A , CM000664.1:g.2843308G>A GRCh37
NC_000002.10:g.2822315G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001739254.1:n.1131+247C>T
XR_001739255.1:n.1124+247C>T