Canonical Allele Identifier: CA615972258
Gene:

Linked Data

dbSNP Id: rs1369625206

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.92307354dup , CM000676.2:g.92307354dup GRCh38
NC_000014.8:g.92773698dup , CM000676.1:g.92773698dup GRCh37
NC_000014.7:g.91843451dup NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_944153.1:n.131+2810dup