Canonical Allele Identifier: CA127194605

Gene: MIR3936HG

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132367886G>C , CM000667.2:g.132367886G>C	GRCh38
NC_000005.9:g.131703578G>C , CM000667.1:g.131703578G>C	GRCh37
NC_000005.8:g.131731477G>C	NCBI36
NG_008982.1:g.3178G>C
NG_008982.2:g.3183G>C

Transcript Alleles

HGVS	Amino-acid Change
NR_110997.1:n.74-1105C>G