Canonical Allele Identifier: CA2246165998
Gene:

Linked Data

dbSNP Id: rs1981897752

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8137839dup , CM000679.2:g.8137839dup GRCh38
NC_000017.10:g.8041157dup , CM000679.1:g.8041157dup GRCh37
NC_000017.9:g.7981882dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_934202.1:n.183-1010dup
XR_934203.1:n.70-1638dup
XR_934202.2:n.414-1010dup