Canonical Allele Identifier: CA1605795009
Gene:

Linked Data

dbSNP Id: rs1761315913

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1535649_1535650dup , CM000668.2:g.1535649_1535650dup GRCh38
NC_000006.11:g.1535884_1535885dup , CM000668.1:g.1535884_1535885dup GRCh37
NC_000006.10:g.1480883_1480884dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_427861.2:n.234+16696_234+16697dup
XR_926380.1:n.218-2807_218-2806dup
XR_926381.1:n.1108-2807_1108-2806dup
XR_926382.1:n.235-6471_235-6470dup
XR_926384.1:n.200-6471_200-6470dup
XR_001743921.1:n.235-6495_235-6494dup
XR_427861.3:n.234+16696_234+16697dup
XR_926381.2:n.1123-2807_1123-2806dup