Canonical Allele Identifier: CA1889344529
Gene:

Linked Data

dbSNP Id: rs1832130401

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.8697585dup , CM000672.2:g.8697585dup GRCh38
NC_000010.10:g.8739548dup , CM000672.1:g.8739548dup GRCh37
NC_000010.9:g.8779554dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930641.1:n.33-27784dup