Canonical Allele Identifier: CA1462694384
Gene:

Linked Data

dbSNP Id: rs1756232688

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62558471del , CM000666.2:g.62558471del GRCh38
NC_000004.11:g.63424189del , CM000666.1:g.63424189del GRCh37
NC_000004.10:g.63106784del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_938814.1:n.161-5373del