Canonical Allele Identifier: CA850516152
Gene:

Linked Data

dbSNP Id: rs1026623291

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.2882987G>T , CM000670.2:g.2882987G>T GRCh38
NC_000008.10:g.2740509G>T , CM000670.1:g.2740509G>T GRCh37
NC_000008.9:g.2727916G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_941367.1:n.212-42778G>T
NR_168441.1:n.1166+45223G>T
NR_168442.1:n.1331-33348G>T
NR_168443.1:n.1171+45223G>T
NR_168444.1:n.1166+45223G>T
NR_168445.1:n.1249+45140G>T