Canonical Allele Identifier: CA615972260
Gene:

Linked Data

dbSNP Id: rs1309025891

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.92307359A>T , CM000676.2:g.92307359A>T GRCh38
NC_000014.8:g.92773703A>T , CM000676.1:g.92773703A>T GRCh37
NC_000014.7:g.91843456A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_944153.1:n.131+2815A>T