Canonical Allele Identifier: CA2675194628
Gene: MIR3936HG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132369645G>T , CM000667.2:g.132369645G>T GRCh38
NC_000005.9:g.131705337G>T , CM000667.1:g.131705337G>T GRCh37
NC_000005.8:g.131733236G>T NCBI36
NG_008982.1:g.4937G>T
NG_008982.2:g.4942G>T

Transcript Alleles

HGVS Amino-acid Change
NR_110997.1:n.73+199C>A