Canonical Allele Identifier: CA963063575
Gene:

Linked Data

dbSNP Id: rs2045894158

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50857024_50857027del , CM000676.2:g.50857024_50857027del GRCh38
NC_000014.8:g.51323742_51323745del , CM000676.1:g.51323742_51323745del GRCh37
NC_000014.7:g.50393492_50393495del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943848.1:n.282+1071_282+1074del
XR_943848.2:n.643+1071_643+1074del