Canonical Allele Identifier: CA2136398929
Gene:

Linked Data

dbSNP Id: rs946828093

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50857027T>A , CM000676.2:g.50857027T>A GRCh38
NC_000014.8:g.51323745T>A , CM000676.1:g.51323745T>A GRCh37
NC_000014.7:g.50393495T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943848.1:n.282+1071A>T
XR_943848.2:n.643+1071A>T