Canonical Allele Identifier: CA1462694180
Gene:

Linked Data

dbSNP Id: rs1756226322

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62558046del , CM000666.2:g.62558046del GRCh38
NC_000004.11:g.63423764del , CM000666.1:g.63423764del GRCh37
NC_000004.10:g.63106359del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938814.1:n.161-5798del