Canonical Allele Identifier: CA150690473
Gene:

Linked Data

dbSNP Id: rs904013485

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155812225_155812228del , CM000668.2:g.155812225_155812228del GRCh38
NC_000006.11:g.156133359_156133362del , CM000668.1:g.156133359_156133362del GRCh37
NC_000006.10:g.156175051_156175054del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943142.1:n.79+18806_79+18809del
XR_943146.1:n.645-185_645-182del
XR_001744423.1:n.699-185_699-182del
XR_001744424.1:n.79+18806_79+18809del