Canonical Allele Identifier: CA127195718
Gene: MIR3936HG HGNC NCBI

Linked Data

dbSNP Id: rs959499927

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132369648C>T , CM000667.2:g.132369648C>T GRCh38
NC_000005.9:g.131705340C>T , CM000667.1:g.131705340C>T GRCh37
NC_000005.8:g.131733239C>T NCBI36
NG_008982.1:g.4940C>T
NG_008982.2:g.4945C>T

Transcript Alleles

HGVS Amino-acid Change
NR_110997.1:n.73+196G>A