Canonical Allele Identifier: CA1583129132
Gene: MIR3936HG HGNC NCBI

Linked Data

dbSNP Id: rs1580857159

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132350353C>T , CM000667.2:g.132350353C>T GRCh38
NC_000005.9:g.131686046C>T , CM000667.1:g.131686046C>T GRCh37
NC_000005.8:g.131713945C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110997.1:n.418-396G>A