Canonical Allele Identifier: CA1605795096
Gene:

Linked Data

dbSNP Id: rs1761320092

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1535885del , CM000668.2:g.1535885del GRCh38
NC_000006.11:g.1536120del , CM000668.1:g.1536120del GRCh37
NC_000006.10:g.1481119del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_427861.2:n.234+16463del
XR_926380.1:n.218-2571del
XR_926381.1:n.1108-2571del
XR_926382.1:n.235-6704del
XR_926384.1:n.200-6704del
XR_001743921.1:n.235-6728del
XR_427861.3:n.234+16463del
XR_926381.2:n.1123-2571del