Canonical Allele Identifier: CA2221132792
Gene:

Linked Data

dbSNP Id: rs1961466669

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.49108606A>G , CM000678.2:g.49108606A>G GRCh38
NC_000016.9:g.49142517A>G , CM000678.1:g.49142517A>G GRCh37
NC_000016.8:g.47700018A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_933517.1:n.810+1338T>C
XR_001752138.2:n.591+5370T>C
XR_933517.2:n.810+1338T>C