Canonical Allele Identifier: CA1583137382
Gene: MIR3936HG HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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