Canonical Allele Identifier: CA709925328
Gene:

Linked Data

dbSNP Id: rs1251633636

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.92307329C>T , CM000676.2:g.92307329C>T GRCh38
NC_000014.8:g.92773673C>T , CM000676.1:g.92773673C>T GRCh37
NC_000014.7:g.91843426C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_944153.1:n.131+2785C>T