Canonical Allele Identifier: CA2269950704
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63498406_63498407delinsCT , CM000679.2:g.63498406_63498407delinsCT GRCh38
NC_000017.10:g.61575767_61575768delinsCT , CM000679.1:g.61575767_61575768delinsCT GRCh37
NC_000017.9:g.58929499_58929500delinsCT NCBI36
NG_011648.1:g.26334_26335delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000577647.2:c.1969+1421_1969+1422delinsCT ENSP00000464149.1:n.1969+1421_1969+1422delinsCT