Canonical Allele Identifier: CA1111564437
Gene:

Linked Data

dbSNP Id: rs1014726476
gnomAD v3: 8-20130260-C-T
gnomAD v4: 8-20130260-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.20130260C>T , CM000670.2:g.20130260C>T GRCh38
NC_000008.10:g.19987771C>T , CM000670.1:g.19987771C>T GRCh37
NC_000008.9:g.20032051C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_949563.1:n.3408+341C>T
XR_949563.2:n.3400+341C>T