Canonical Allele Identifier: CA1889449129
Gene:

Linked Data

dbSNP Id: rs1834855330

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.9011191_9011193dup , CM000672.2:g.9011191_9011193dup GRCh38
NC_000010.10:g.9053154_9053156dup , CM000672.1:g.9053154_9053156dup GRCh37
NC_000010.9:g.9093160_9093162dup NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930641.1:n.32+54170_32+54172dup