Canonical Allele Identifier: CA562767590
Gene: MIR3936HG HGNC NCBI

Linked Data

dbSNP Id: rs1176581185

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132369631A>C , CM000667.2:g.132369631A>C GRCh38
NC_000005.9:g.131705323A>C , CM000667.1:g.131705323A>C GRCh37
NC_000005.8:g.131733222A>C NCBI36
NG_008982.1:g.4923A>C
NG_008982.2:g.4928A>C

Transcript Alleles

HGVS Amino-acid Change
NR_110997.1:n.73+213T>G