Canonical Allele Identifier: CA2341104184
Gene:

Linked Data

dbSNP Id: rs2090049941

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50837477_50837482del , CM000681.2:g.50837477_50837482del GRCh38
NC_000019.9:g.51340733_51340738del , CM000681.1:g.51340733_51340738del GRCh37
NC_000019.8:g.56032545_56032550del NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_131203.1:n.213+6184_213+6189del
NR_131205.1:n.230+6184_230+6189del
XR_936030.1:n.298+6184_298+6189del
XR_936031.1:n.298+6184_298+6189del
XR_936032.1:n.298+6184_298+6189del
XR_936033.1:n.294+6184_294+6189del
XR_936035.1:n.281+6184_281+6189del