Canonical Allele Identifier: CA1583137327
Gene: MIR3936HG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132369577C= , CM000667.2:g.132369577C= GRCh38
NC_000005.9:g.131705269C= , CM000667.1:g.131705269C= GRCh37
NC_000005.8:g.131733168C= NCBI36
NG_008982.1:g.4869C=
NG_008982.2:g.4874C=

Transcript Alleles

HGVS Amino-acid Change
NR_110997.1:n.73+267G=