Canonical Allele Identifier: CA821226191
Gene:

Linked Data

dbSNP Id: rs1339450549

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155817528_155817533dup , CM000668.2:g.155817528_155817533dup GRCh38
NC_000006.11:g.156138662_156138667dup , CM000668.1:g.156138662_156138667dup GRCh37
NC_000006.10:g.156180354_156180359dup NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943142.1:n.79+24109_79+24114dup
XR_943146.1:n.552-2863_552-2858dup
XR_001744423.1:n.606-2863_606-2858dup
XR_001744424.1:n.79+24109_79+24114dup