Canonical Allele Identifier: CA2675194720
Gene: MIR3936HG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132369693C>G , CM000667.2:g.132369693C>G GRCh38
NC_000005.9:g.131705385C>G , CM000667.1:g.131705385C>G GRCh37
NC_000005.8:g.131733284C>G NCBI36
NG_008982.1:g.4985C>G
NG_008982.2:g.4990C>G

Transcript Alleles

HGVS Amino-acid Change
NR_110997.1:n.73+151G>C