Canonical Allele Identifier: CA965992677
Gene:

Linked Data

dbSNP Id: rs1884565837

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.92307351T>C , CM000676.2:g.92307351T>C GRCh38
NC_000014.8:g.92773695T>C , CM000676.1:g.92773695T>C GRCh37
NC_000014.7:g.91843448T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_944153.1:n.131+2807T>C