Canonical Allele Identifier: CA784842247
Gene:

Linked Data

dbSNP Id: rs1174803337

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542489del , CM000666.2:g.105542489del GRCh38
NC_000004.11:g.106463646del , CM000666.1:g.106463646del GRCh37
NC_000004.10:g.106683095del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939038.1:n.516del
XR_939039.1:n.676del
XR_939040.1:n.296-1013del
XR_001741410.1:n.531del
XR_001741411.1:n.1007del
XR_001741412.1:n.449+82del
XR_001741413.1:n.531del
XR_001741414.1:n.449+82del
XR_939038.2:n.531del
XR_939040.2:n.311-1013del