Canonical Allele Identifier: CA2729922498
Gene:

Linked Data

dbSNP Id: rs1884673494

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.92314516C>T , CM000676.2:g.92314516C>T GRCh38
NC_000014.8:g.92780860C>T , CM000676.1:g.92780860C>T GRCh37
NC_000014.7:g.91850613C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_944153.1:n.132-730C>T