Canonical Allele Identifier: CA2346122828
Gene:

Linked Data

dbSNP Id: rs2085112726

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.2471033del , CM000682.2:g.2471033del GRCh38
NC_000020.10:g.2451679del , CM000682.1:g.2451679del GRCh37
NC_000020.9:g.2399679del NCBI36
NG_042057.1:g.4822del

Transcript Alleles

HGVS Amino-acid Change
ENST00000461548.1:c.305-3274del ENSP00000456213.1:n.305-3274del