Canonical Allele Identifier: CA202824886

Gene:

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.9007290C>G , CM000672.2:g.9007290C>G	GRCh38
NC_000010.10:g.9049253C>G , CM000672.1:g.9049253C>G	GRCh37
NC_000010.9:g.9089259C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_930641.1:n.32+58073G>C