Canonical Allele Identifier: CA821943357
Gene:

Linked Data

dbSNP Id: rs1166563832

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.163765684del , CM000668.2:g.163765684del GRCh38
NC_000006.11:g.164186716del , CM000668.1:g.164186716del GRCh37
NC_000006.10:g.164106706del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001744452.1:n.410+6255del
XR_001744454.1:n.369+6296del
XR_001744455.1:n.346+6319del