Canonical Allele Identifier: CA803979832

Gene: MIR3936HG

Linked Data

• dbSNP Id: rs914901811
• MyVariant Identifiers: chr5:g.131705207G>A (hg19) ; chr5:g.132369515G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132369515G>A , CM000667.2:g.132369515G>A	GRCh38
NC_000005.9:g.131705207G>A , CM000667.1:g.131705207G>A	GRCh37
NC_000005.8:g.131733106G>A	NCBI36
NG_008982.1:g.4807G>A
NG_008982.2:g.4812G>A

Transcript Alleles

HGVS	Amino-acid Change
NR_110997.1:n.73+329C>T