Canonical Allele Identifier: CA2722920721

Gene:

Linked Data

• dbSNP Id: rs2133901439

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.122458389_122458390insGGGA , CM000672.2:g.122458389_122458390insGGGA	GRCh38
NC_000010.10:g.124217905_124217906insGGGA , CM000672.1:g.124217905_124217906insGGGA	GRCh37
NC_000010.9:g.124207895_124207896insGGGA	NCBI36
NG_011554.1:g.1865_1866insGGGA
NG_011725.1:g.8727_8728insGGGA

Transcript Alleles

HGVS	Amino-acid Change
XR_946382.1:n.1827+107_1827+108insCCTC
XR_946383.1:n.1827+107_1827+108insCCTC
XR_946384.1:n.1576+107_1576+108insCCTC
XR_946385.1:n.1827+107_1827+108insCCTC
XR_946382.2:n.1855+107_1855+108insCCTC
XR_946383.2:n.1855+107_1855+108insCCTC
XR_946384.2:n.1580+107_1580+108insCCTC
XR_946385.2:n.1855+107_1855+108insCCTC