Canonical Allele Identifier: CA122896014
Gene:

Linked Data

dbSNP Id: rs894004193
gnomAD v2: 5-91518631-C-T
gnomAD v3: 5-92222814-C-T
gnomAD v4: 5-92222814-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.92222814C>T , CM000667.2:g.92222814C>T GRCh38
NC_000005.9:g.91518631C>T , CM000667.1:g.91518631C>T GRCh37
NC_000005.8:g.91554387C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_948565.1:n.394+18130C>T