Canonical Allele Identifier: CA1912720899
Gene:

Linked Data

dbSNP Id: rs1839461727

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.57812849_57812850insCCA , CM000672.2:g.57812849_57812850insCCA GRCh38
NC_000010.10:g.59572609_59572610insCCA , CM000672.1:g.59572609_59572610insCCA GRCh37
NC_000010.9:g.59242615_59242616insCCA NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_945979.1:n.68+34442_68+34443insTGG
XR_001747454.1:n.85+34442_85+34443insTGG