Canonical Allele Identifier: CA144319783
Gene:

Linked Data

dbSNP Id: rs34104748

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98102461dup , CM000668.2:g.98102461dup GRCh38
NC_000006.11:g.98550337dup , CM000668.1:g.98550337dup GRCh37
NC_000006.10:g.98657058dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245563.2:n.456+3191dup
XR_942809.1:n.456+3191dup