Canonical Allele Identifier: CA2675194602
Gene: MIR3936HG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132369628G>C , CM000667.2:g.132369628G>C GRCh38
NC_000005.9:g.131705320G>C , CM000667.1:g.131705320G>C GRCh37
NC_000005.8:g.131733219G>C NCBI36
NG_008982.1:g.4920G>C
NG_008982.2:g.4925G>C

Transcript Alleles

HGVS Amino-acid Change
NR_110997.1:n.73+216C>G