Canonical Allele Identifier: CA914909825
Gene:

Linked Data

dbSNP Id: rs1560232896

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.12578091del , CM000666.2:g.12578091del GRCh38
NC_000004.11:g.12579715del , CM000666.1:g.12579715del GRCh37
NC_000004.10:g.12188813del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_925406.1:n.106+31251del
XR_001741374.1:n.254+44564del
XR_925406.3:n.140+31251del