Canonical Allele Identifier: CA1149683783
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2567438_2567439delinsAG , CM000663.2:g.2567438_2567439delinsAG GRCh38
NC_000001.10:g.2498877_2498878delinsAG , CM000663.1:g.2498877_2498878delinsAG GRCh37
NC_000001.9:g.2475540_2475541delinsCT NCBI36
NG_047096.1:g.16074_16075delinsAG

Transcript Alleles

HGVS Amino-acid change
NR_121638.1:n.71+833_71+834delinsAG