Canonical Allele Identifier: CA526771941
Gene:

Linked Data

dbSNP Id: rs1553198044

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168649339del , CM000663.2:g.168649339del GRCh38
NC_000001.10:g.168618577del , CM000663.1:g.168618577del GRCh37
NC_000001.9:g.166885201del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_922259.1:n.201-8061del
XR_922259.2:n.332-8061del