Canonical Allele Identifier: CA784842379
Gene:

Linked Data

dbSNP Id: rs1290146651

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542757del , CM000666.2:g.105542757del GRCh38
NC_000004.11:g.106463914del , CM000666.1:g.106463914del GRCh37
NC_000004.10:g.106683363del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.296-48del
XR_939039.1:n.456-48del
XR_939040.1:n.296-1281del
XR_001741410.1:n.311-48del
XR_001741411.1:n.787-48del
XR_001741412.1:n.311-48del
XR_001741413.1:n.311-48del
XR_001741414.1:n.311-48del
XR_939038.2:n.311-48del
XR_939040.2:n.311-1281del