Canonical Allele Identifier: CA1905920016
Gene:

Linked Data

dbSNP Id: rs1837179591

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43318642del , CM000672.2:g.43318642del GRCh38
NC_000010.10:g.43814090del , CM000672.1:g.43814090del GRCh37
NC_000010.9:g.43134096del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945902.1:n.108+47del
XR_945902.2:n.198+47del