Canonical Allele Identifier: CA2604424663
Gene: MIR3936HG HGNC NCBI

Linked Data

dbSNP Id: rs2126753423

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132350174G>T , CM000667.2:g.132350174G>T GRCh38
NC_000005.9:g.131685867G>T , CM000667.1:g.131685867G>T GRCh37
NC_000005.8:g.131713766G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110997.1:n.418-217C>A