Canonical Allele Identifier: CA2497475791

Gene:

Linked Data

• dbSNP Id: rs1804274805

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31176591_31176593dup , CM000670.2:g.31176591_31176593dup	GRCh38
NC_000008.10:g.31034107_31034109dup , CM000670.1:g.31034107_31034109dup	GRCh37
NC_000008.9:g.31153649_31153651dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_949642.1:n.270+2_270+4dup
XR_949643.1:n.87+100_87+102dup
XR_949644.1:n.87+100_87+102dup
XR_949645.1:n.87+100_87+102dup
XR_949646.1:n.87+100_87+102dup
XR_949647.1:n.700+100_700+102dup
XR_949648.1:n.602+100_602+102dup