Canonical Allele Identifier: CA552053308
Gene:

Linked Data

dbSNP Id: rs1352287303

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62558490del , CM000666.2:g.62558490del GRCh38
NC_000004.11:g.63424208del , CM000666.1:g.63424208del GRCh37
NC_000004.10:g.63106803del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938814.1:n.161-5354del