Canonical Allele Identifier: CA1081634995
Gene: MIR3936HG HGNC NCBI

Linked Data

dbSNP Id: rs1444455469

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132369556G>A , CM000667.2:g.132369556G>A GRCh38
NC_000005.9:g.131705248G>A , CM000667.1:g.131705248G>A GRCh37
NC_000005.8:g.131733147G>A NCBI36
NG_008982.1:g.4848G>A
NG_008982.2:g.4853G>A

Transcript Alleles

HGVS Amino-acid Change
NR_110997.1:n.73+288C>T