Canonical Allele Identifier: CA2136398915
Gene:

Linked Data

dbSNP Id: rs2045894029

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50856997G>A , CM000676.2:g.50856997G>A GRCh38
NC_000014.8:g.51323715G>A , CM000676.1:g.51323715G>A GRCh37
NC_000014.7:g.50393465G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943848.1:n.282+1101C>T
XR_943848.2:n.643+1101C>T