Canonical Allele Identifier: CA265579796
Gene:

Linked Data

dbSNP Id: rs988203020

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.92307394C>T , CM000676.2:g.92307394C>T GRCh38
NC_000014.8:g.92773738C>T , CM000676.1:g.92773738C>T GRCh37
NC_000014.7:g.91843491C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_944153.1:n.131+2850C>T