Canonical Allele Identifier: CA918778951
Gene:

Linked Data

dbSNP Id: rs1554947719

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122458386_122458387insG , CM000672.2:g.122458386_122458387insG GRCh38
NC_000010.10:g.124217902_124217903insG , CM000672.1:g.124217902_124217903insG GRCh37
NC_000010.9:g.124207892_124207893insG NCBI36
NG_011554.1:g.1862_1863insG
NG_011725.1:g.8724_8725insG

Transcript Alleles

HGVS Amino-acid Change
XR_946382.1:n.1827+108_1827+109insC
XR_946383.1:n.1827+108_1827+109insC
XR_946384.1:n.1576+108_1576+109insC
XR_946385.1:n.1827+108_1827+109insC
XR_946382.2:n.1855+108_1855+109insC
XR_946383.2:n.1855+108_1855+109insC
XR_946384.2:n.1580+108_1580+109insC
XR_946385.2:n.1855+108_1855+109insC