Canonical Allele Identifier: CA127211574

Gene: MIR3936HG

Linked Data

• dbSNP Id: rs914716025
• MyVariant Identifiers: chr5:g.131686065A>G (hg19) ; chr5:g.132350372A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132350372A>G , CM000667.2:g.132350372A>G	GRCh38
NC_000005.9:g.131686065A>G , CM000667.1:g.131686065A>G	GRCh37
NC_000005.8:g.131713964A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_110997.1:n.418-415T>C