Canonical Allele Identifier: CA916908016
Gene:

Linked Data

dbSNP Id: rs1576348723

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.61428192del , CM000665.2:g.61428192del GRCh38
NC_000003.11:g.61413866del , CM000665.1:g.61413866del GRCh37
NC_000003.10:g.61388906del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_940892.1:n.164+325del
XR_940893.1:n.164+325del
XR_001740725.1:n.202+325del
XR_940892.2:n.202+325del