Canonical Allele Identifier: CA1021127353
Gene:

Linked Data

dbSNP Id: rs1981482773

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.22259403del , CM000683.2:g.22259403del GRCh38
NC_000021.8:g.23631723del , CM000683.1:g.23631723del GRCh37
NC_000021.7:g.22553594del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001754978.1:n.221+46590del