Canonical Allele Identifier: CA2710221001
Gene: MIR3936HG HGNC NCBI

Linked Data

dbSNP Id: rs2126763819

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132369547T>G , CM000667.2:g.132369547T>G GRCh38
NC_000005.9:g.131705239T>G , CM000667.1:g.131705239T>G GRCh37
NC_000005.8:g.131733138T>G NCBI36
NG_008982.1:g.4839T>G
NG_008982.2:g.4844T>G

Transcript Alleles

HGVS Amino-acid Change
NR_110997.1:n.73+297A>C