Canonical Allele Identifier: CA170474085
Gene:

Linked Data

dbSNP Id: rs952313564
gnomAD v3: 8-2180484-G-T
gnomAD v4: 8-2180484-G-T
MyVariant Identifiers: chr8:g.2180484G>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.2180484G>T , CM000670.2:g.2180484G>T GRCh38
NC_000008.9:g.2116094G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_941356.1:n.112-12451G>T
XR_941355.2:n.133-3540G>T
XR_941356.2:n.133-12451G>T