Canonical Allele Identifier: CA965996455
Gene:

Linked Data

dbSNP Id: rs1884673987

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.92314560A>T , CM000676.2:g.92314560A>T GRCh38
NC_000014.8:g.92780904A>T , CM000676.1:g.92780904A>T GRCh37
NC_000014.7:g.91850657A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_944153.1:n.132-686A>T