Canonical Allele Identifier: CA170573746
Gene:

Linked Data

dbSNP Id: rs919384168
gnomAD v3: 8-2883001-C-T
gnomAD v4: 8-2883001-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.2883001C>T , CM000670.2:g.2883001C>T GRCh38
NC_000008.10:g.2740523C>T , CM000670.1:g.2740523C>T GRCh37
NC_000008.9:g.2727930C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_941367.1:n.212-42764C>T
NR_168441.1:n.1166+45237C>T
NR_168442.1:n.1331-33334C>T
NR_168443.1:n.1171+45237C>T
NR_168444.1:n.1166+45237C>T
NR_168445.1:n.1249+45154C>T