Canonical Allele Identifier: CA220638142
Gene:

Linked Data

dbSNP Id: rs79892222

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.34759256del , CM000673.2:g.34759256del GRCh38
NC_000011.9:g.34780803del , CM000673.1:g.34780803del GRCh37
NC_000011.8:g.34737379del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_428897.2:n.579+4649del
XR_931188.1:n.693+4649del
XR_931189.1:n.854+4649del
XR_931190.1:n.639+4649del
XR_931191.1:n.689+4649del
XR_001748174.1:n.855+4649del
XR_001748176.1:n.1016+4649del
XR_002957246.1:n.639+4649del