Canonical Allele Identifier: CA1583137386
Gene: MIR3936HG HGNC NCBI

Linked Data

dbSNP Id: rs922384304

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132369691C>T , CM000667.2:g.132369691C>T GRCh38
NC_000005.9:g.131705383C>T , CM000667.1:g.131705383C>T GRCh37
NC_000005.8:g.131733282C>T NCBI36
NG_008982.1:g.4983C>T
NG_008982.2:g.4988C>T

Transcript Alleles

HGVS Amino-acid Change
NR_110997.1:n.73+153G>A