Canonical Allele Identifier: CA200491637
Gene:

Linked Data

dbSNP Id: rs62584730

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.129576779C>T , CM000671.2:g.129576779C>T GRCh38
NC_000009.11:g.132339058C>T , CM000671.1:g.132339058C>T GRCh37
NC_000009.10:g.131378879C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930390.1:n.182+1181C>T