Canonical Allele Identifier: CA2675194746
Gene: MIR3936HG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132369703C>T , CM000667.2:g.132369703C>T GRCh38
NC_000005.9:g.131705395C>T , CM000667.1:g.131705395C>T GRCh37
NC_000005.8:g.131733294C>T NCBI36
NG_008982.1:g.4995C>T
NG_008982.2:g.5000C>T

Transcript Alleles

HGVS Amino-acid Change
NR_110997.1:n.73+141G>A