Canonical Allele Identifier: CA1760507485

Gene:

Linked Data

• dbSNP Id: rs1798571677

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.5907113_5907114del , CM000670.2:g.5907113_5907114del	GRCh38
NC_000008.10:g.5764635_5764636del , CM000670.1:g.5764635_5764636del	GRCh37
NC_000008.9:g.5752043_5752044del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_941374.1:n.308-7381_308-7380del
XR_941375.1:n.308-7381_308-7380del
XR_941376.1:n.406-7381_406-7380del
XR_941377.1:n.308-7381_308-7380del
XR_941378.1:n.216-7381_216-7380del
XR_001745765.1:n.308-7381_308-7380del
XR_001745766.1:n.406-7381_406-7380del
XR_001745767.1:n.216-7381_216-7380del
XR_001745768.1:n.308-7381_308-7380del
XR_941374.2:n.308-7381_308-7380del
XR_941375.2:n.308-7381_308-7380del