Canonical Allele Identifier: CA260835420
Gene:

Linked Data

dbSNP Id: rs891509176
MyVariant Identifiers: chr14:g.50856836T>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50856836T>A , CM000676.2:g.50856836T>A GRCh38
NC_000014.8:g.51323554T>A , CM000676.1:g.51323554T>A GRCh37
NC_000014.7:g.50393304T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943848.1:n.282+1262A>T
XR_943848.2:n.643+1262A>T