Canonical Allele Identifier: CA2675194618
Gene: MIR3936HG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132369639A>T , CM000667.2:g.132369639A>T GRCh38
NC_000005.9:g.131705331A>T , CM000667.1:g.131705331A>T GRCh37
NC_000005.8:g.131733230A>T NCBI36
NG_008982.1:g.4931A>T
NG_008982.2:g.4936A>T

Transcript Alleles

HGVS Amino-acid Change
NR_110997.1:n.73+205T>A