Canonical Allele Identifier: CA13102361
Gene:

Linked Data

dbSNP Id: rs10988428

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.129576791G>T , CM000671.2:g.129576791G>T GRCh38
NC_000009.11:g.132339070G>T , CM000671.1:g.132339070G>T GRCh37
NC_000009.10:g.131378891G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930390.1:n.182+1193G>T