Canonical Allele Identifier: CA310819065
Gene:

Linked Data

dbSNP Id: rs199910116

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.1875501_1875504del , CM000682.2:g.1875501_1875504del GRCh38
NC_000020.10:g.1856147_1856150del , CM000682.1:g.1856147_1856150del GRCh37
NC_000020.9:g.1804147_1804150del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001754467.1:n.433-7410_433-7407del