Canonical Allele Identifier: CA1886690291
Gene:

Linked Data

dbSNP Id: rs1831781534

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.3366800C>G , CM000672.2:g.3366800C>G GRCh38
NC_000010.10:g.3408992C>G , CM000672.1:g.3408992C>G GRCh37
NC_000010.9:g.3398992C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_131187.1:n.162+47944C>G