Canonical Allele Identifier: CA1149396873
Gene:

Linked Data

dbSNP Id: rs1659179461

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2036381_2036382del , CM000663.2:g.2036381_2036382del GRCh38
NC_000001.10:g.1967820_1967821del , CM000663.1:g.1967820_1967821del GRCh37
NC_000001.9:g.1957680_1957681del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_946823.1:n.773+55_773+56del
XR_001737845.2:n.831_832del
XR_946823.3:n.776+55_776+56del