Canonical Allele Identifier: CA2675194470
Gene: MIR3936HG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132369530A>G , CM000667.2:g.132369530A>G GRCh38
NC_000005.9:g.131705222A>G , CM000667.1:g.131705222A>G GRCh37
NC_000005.8:g.131733121A>G NCBI36
NG_008982.1:g.4822A>G
NG_008982.2:g.4827A>G

Transcript Alleles

HGVS Amino-acid Change
NR_110997.1:n.73+314T>C