Canonical Allele Identifier: CA890857285
Gene:

Linked Data

dbSNP Id: rs1184991747

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168649440del , CM000663.2:g.168649440del GRCh38
NC_000001.10:g.168618678del , CM000663.1:g.168618678del GRCh37
NC_000001.9:g.166885302del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_922259.1:n.201-8163del
XR_922259.2:n.332-8163del