Canonical Allele Identifier: CA920151958
Gene:

Linked Data

dbSNP Id: rs1555757544

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.2470861del , CM000682.2:g.2470861del GRCh38
NC_000020.10:g.2451507del , CM000682.1:g.2451507del GRCh37
NC_000020.9:g.2399507del NCBI36
NG_042057.1:g.4996del

Transcript Alleles

HGVS Amino-acid Change
ENST00000461548.1:c.305-3100del ENSP00000456213.1:n.305-3100del