Canonical Allele Identifier: CA965996474
Gene:

Linked Data

dbSNP Id: rs1884674820

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.92314630A>G , CM000676.2:g.92314630A>G GRCh38
NC_000014.8:g.92780974A>G , CM000676.1:g.92780974A>G GRCh37
NC_000014.7:g.91850727A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_944153.1:n.132-616A>G