Canonical Allele Identifier: CA918191840

Gene:

Linked Data

• dbSNP Id: rs1554459219

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.5907566_5907567delinsG , CM000670.2:g.5907566_5907567delinsG	GRCh38
NC_000008.10:g.5765088_5765089delinsG , CM000670.1:g.5765088_5765089delinsG	GRCh37
NC_000008.9:g.5752496_5752497delinsG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_941374.1:n.308-7836_308-7835delinsC
XR_941375.1:n.308-7836_308-7835delinsC
XR_941376.1:n.406-7836_406-7835delinsC
XR_941377.1:n.308-7836_308-7835delinsC
XR_941378.1:n.216-7836_216-7835delinsC
XR_001745765.1:n.308-7836_308-7835delinsC
XR_001745766.1:n.406-7836_406-7835delinsC
XR_001745767.1:n.216-7836_216-7835delinsC
XR_001745768.1:n.308-7836_308-7835delinsC
XR_941374.2:n.308-7836_308-7835delinsC
XR_941375.2:n.308-7836_308-7835delinsC