Canonical Allele Identifier: CA1839056735
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21756068_21756071delinsCCTT , CM000671.2:g.21756068_21756071delinsCCTT GRCh38
NC_000009.11:g.21756067_21756070delinsCCTT , CM000671.1:g.21756067_21756070delinsCCTT GRCh37
NC_000009.10:g.21746067_21746070delinsCCTT NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001746563.2:n.163+11754_163+11757delinsAAGG