Canonical Allele Identifier: CA2710055888
Gene: MIR3936HG HGNC NCBI

Linked Data

dbSNP Id: rs959499927

Genomic Alleles

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

Transcript Alleles

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