Canonical Allele Identifier: CA2059284977
Gene:

Linked Data

dbSNP Id: rs1566017400

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102501318C>T , CM000674.2:g.102501318C>T GRCh38
NC_000012.11:g.102895096C>T , CM000674.1:g.102895096C>T GRCh37
NC_000012.10:g.101419226C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001749289.1:n.1952+17430C>T