Canonical Allele Identifier: CA2733843046
Gene:

Linked Data

dbSNP Id: rs2144613968

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50211613_50211614insAAAA , CM000679.2:g.50211613_50211614insAAAA GRCh38
NC_000017.10:g.48288974_48288975insAAAA , CM000679.1:g.48288974_48288975insAAAA GRCh37
NC_000017.9:g.45643973_45643974insAAAA NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_934838.1:n.42+2207_42+2208insAAAA