Canonical Allele Identifier: CA551536785
Gene:

Linked Data

dbSNP Id: rs796931887

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.54072315del , CM000666.2:g.54072315del GRCh38
NC_000004.11:g.54938482del , CM000666.1:g.54938482del GRCh37
NC_000004.10:g.54633239del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000507166.5:c.1018-202610del ENSP00000423325.1:n.1018-202610del