Canonical Allele Identifier: CA2675194682
Gene: MIR3936HG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132369676C>A , CM000667.2:g.132369676C>A GRCh38
NC_000005.9:g.131705368C>A , CM000667.1:g.131705368C>A GRCh37
NC_000005.8:g.131733267C>A NCBI36
NG_008982.1:g.4968C>A
NG_008982.2:g.4973C>A

Transcript Alleles

HGVS Amino-acid Change
NR_110997.1:n.73+168G>T