Canonical Allele Identifier: CA1583129193
Gene: MIR3936HG HGNC NCBI

Linked Data

dbSNP Id: rs1580857225

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132350562C>T , CM000667.2:g.132350562C>T GRCh38
NC_000005.9:g.131686255C>T , CM000667.1:g.131686255C>T GRCh37
NC_000005.8:g.131714154C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110997.1:n.418-605G>A