Canonical Allele Identifier: CA12063673

Gene: MIR3936HG

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132358913G>A , CM000667.2:g.132358913G>A	GRCh38
NC_000005.9:g.131694606G>A , CM000667.1:g.131694606G>A	GRCh37
NC_000005.8:g.131722505G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_110997.1:n.417+1167C>T