Canonical Allele Identifier: CA1800733891
Gene:

Linked Data

dbSNP Id: rs1810442986

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.88535794A>G , CM000670.2:g.88535794A>G GRCh38
NC_000008.10:g.89548023A>G , CM000670.1:g.89548023A>G GRCh37
NC_000008.9:g.89617139A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001745651.2:n.1673+10723T>C
XR_001745653.2:n.286-6886A>G
XR_928383.3:n.1475+10723T>C