Canonical Allele Identifier: CA127195736
Gene: MIR3936HG HGNC NCBI

Linked Data

dbSNP Id: rs749828528

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132369681C>A , CM000667.2:g.132369681C>A GRCh38
NC_000005.9:g.131705373C>A , CM000667.1:g.131705373C>A GRCh37
NC_000005.8:g.131733272C>A NCBI36
NG_008982.1:g.4973C>A
NG_008982.2:g.4978C>A

Transcript Alleles

HGVS Amino-acid Change
NR_110997.1:n.73+163G>T