Canonical Allele Identifier: CA704082271
Gene:

Linked Data

dbSNP Id: rs1171677045

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.20793554del , CM000676.2:g.20793554del GRCh38
NC_000014.8:g.21261713del , CM000676.1:g.21261713del GRCh37
NC_000014.7:g.20331553del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943584.1:n.585+768del
XR_943585.1:n.585+768del
XR_001750620.1:n.3271+768del
XR_001750621.1:n.3271+768del
XR_001750622.1:n.637+6353del
XR_001750623.1:n.637+6353del
XR_001750624.1:n.637+6353del