Canonical Allele Identifier: CA127211578

Gene: MIR3936HG

Linked Data

• dbSNP Id: rs988192066
• MyVariant Identifiers: chr5:g.132350380G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132350380G>T , CM000667.2:g.132350380G>T	GRCh38
NC_000005.9:g.131686073G>T , CM000667.1:g.131686073G>T	GRCh37
NC_000005.8:g.131713972G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_110997.1:n.418-423C>A