Canonical Allele Identifier: CA1247519139
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.41534676_41534677delinsAG , CM000664.2:g.41534676_41534677delinsAG GRCh38
NC_000002.11:g.41761816_41761817delinsAG , CM000664.1:g.41761816_41761817delinsAG GRCh37
NC_000002.10:g.41615320_41615321delinsAG NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939996.1:n.181+3049_181+3050delinsCT
XR_939997.1:n.146+3049_146+3050delinsCT
XR_939997.2:n.9529+3049_9529+3050delinsCT