Canonical Allele Identifier: CA2675194626
Gene: MIR3936HG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132369644A>T , CM000667.2:g.132369644A>T GRCh38
NC_000005.9:g.131705336A>T , CM000667.1:g.131705336A>T GRCh37
NC_000005.8:g.131733235A>T NCBI36
NG_008982.1:g.4936A>T
NG_008982.2:g.4941A>T

Transcript Alleles

HGVS Amino-acid Change
NR_110997.1:n.73+200T>A