Canonical Allele Identifier: CA170573747
Gene:

Linked Data

dbSNP Id: rs543694489

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.2883008G>T , CM000670.2:g.2883008G>T GRCh38
NC_000008.10:g.2740530G>T , CM000670.1:g.2740530G>T GRCh37
NC_000008.9:g.2727937G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_941367.1:n.212-42757G>T
NR_168441.1:n.1166+45244G>T
NR_168442.1:n.1331-33327G>T
NR_168443.1:n.1171+45244G>T
NR_168444.1:n.1166+45244G>T
NR_168445.1:n.1249+45161G>T