Canonical Allele Identifier: CA1319876341
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.198767769_198767770delinsCT , CM000664.2:g.198767769_198767770delinsCT GRCh38
NC_000002.11:g.199632493_199632494delinsCT , CM000664.1:g.199632493_199632494delinsCT GRCh37
NC_000002.10:g.199340738_199340739delinsCT NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923758.1:n.72+4489_72+4490delinsAG
XR_923759.1:n.72+4489_72+4490delinsAG
XR_923760.1:n.72+4489_72+4490delinsAG
XR_923759.2:n.72+4489_72+4490delinsAG
XR_923760.2:n.72+4489_72+4490delinsAG