Canonical Allele Identifier: CA191701706
Gene:

Linked Data

dbSNP Id: rs776068457

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.25551430del , CM000671.2:g.25551430del GRCh38
NC_000009.11:g.25551428del , CM000671.1:g.25551428del GRCh37
NC_000009.10:g.25541428del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_929525.1:n.50-853del
XR_929525.2:n.674-853del