Canonical Allele Identifier: CA950572656
Gene:

Linked Data

dbSNP Id: rs1873067524

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.93293190del , CM000674.2:g.93293190del GRCh38
NC_000012.11:g.93686966del , CM000674.1:g.93686966del GRCh37
NC_000012.10:g.92211097del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040096.1:n.329+34838del