Canonical Allele Identifier: CA918778946

Gene:

Linked Data

• dbSNP Id: rs869206576

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.122458388_122458390del , CM000672.2:g.122458388_122458390del	GRCh38
NC_000010.10:g.124217904_124217906del , CM000672.1:g.124217904_124217906del	GRCh37
NC_000010.9:g.124207894_124207896del	NCBI36
NG_011554.1:g.1864_1866del
NG_011725.1:g.8726_8728del

Transcript Alleles

HGVS	Amino-acid Change
XR_946382.1:n.1827+107_1827+109del
XR_946383.1:n.1827+107_1827+109del
XR_946384.1:n.1576+107_1576+109del
XR_946385.1:n.1827+107_1827+109del
XR_946382.2:n.1855+107_1855+109del
XR_946383.2:n.1855+107_1855+109del
XR_946384.2:n.1580+107_1580+109del
XR_946385.2:n.1855+107_1855+109del