Canonical Allele Identifier: CA1583137385
Gene: MIR3936HG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132369691C= , CM000667.2:g.132369691C= GRCh38
NC_000005.9:g.131705383C= , CM000667.1:g.131705383C= GRCh37
NC_000005.8:g.131733282C= NCBI36
NG_008982.1:g.4983C=
NG_008982.2:g.4988C=

Transcript Alleles

HGVS Amino-acid Change
NR_110997.1:n.73+153G=