Canonical Allele Identifier: CA2675194459
Gene: MIR3936HG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132369516A>G , CM000667.2:g.132369516A>G GRCh38
NC_000005.9:g.131705208A>G , CM000667.1:g.131705208A>G GRCh37
NC_000005.8:g.131733107A>G NCBI36
NG_008982.1:g.4808A>G
NG_008982.2:g.4813A>G

Transcript Alleles

HGVS Amino-acid Change
NR_110997.1:n.73+328T>C