Canonical Allele Identifier: CA207989726
Gene:

Linked Data

dbSNP Id: rs1011414140

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.57812853_57812854dup , CM000672.2:g.57812853_57812854dup GRCh38
NC_000010.10:g.59572613_59572614dup , CM000672.1:g.59572613_59572614dup GRCh37
NC_000010.9:g.59242619_59242620dup NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_945979.1:n.68+34447_68+34448dup
XR_001747454.1:n.85+34447_85+34448dup