Canonical Allele Identifier: CA1583137292
Gene: MIR3936HG HGNC NCBI

Linked Data

dbSNP Id: rs1580866314

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132369521C>G , CM000667.2:g.132369521C>G GRCh38
NC_000005.9:g.131705213C>G , CM000667.1:g.131705213C>G GRCh37
NC_000005.8:g.131733112C>G NCBI36
NG_008982.1:g.4813C>G
NG_008982.2:g.4818C>G

Transcript Alleles

HGVS Amino-acid Change
NR_110997.1:n.73+323G>C