Canonical Allele Identifier: CA742240653
Gene:

Linked Data

dbSNP Id: rs1292546020

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23661844T>A , CM000682.2:g.23661844T>A GRCh38
NC_000020.10:g.23642481T>A , CM000682.1:g.23642481T>A GRCh37
NC_000020.9:g.23590481T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001754712.1:n.280+194T>A