Canonical Allele Identifier: CA1116942020
Gene:

Linked Data

gnomAD v3: 8-97269629-C-A
gnomAD v4: 8-97269629-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.97269629C>A , CM000670.2:g.97269629C>A GRCh38
NC_000008.10:g.98281857C>A , CM000670.1:g.98281857C>A GRCh37
NC_000008.9:g.98351033C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_125390.1:n.471+149441G>T