Canonical Allele Identifier: CA1305906793
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.168260559_168260564delinsGTCCTT , CM000664.2:g.168260559_168260564delinsGTCCTT GRCh38
NC_000002.11:g.169117069_169117074delinsGTCCTT , CM000664.1:g.169117069_169117074delinsGTCCTT GRCh37
NC_000002.10:g.168825315_168825320delinsGTCCTT NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001739763.1:n.912-4537_912-4532delinsGTCCTT
XR_001739764.1:n.318-4537_318-4532delinsGTCCTT
XR_001739765.1:n.436-4537_436-4532delinsGTCCTT