Canonical Allele Identifier: CA127195735
Gene: MIR3936HG HGNC NCBI

Linked Data

dbSNP Id: rs574276546

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132369673C>G , CM000667.2:g.132369673C>G GRCh38
NC_000005.9:g.131705365C>G , CM000667.1:g.131705365C>G GRCh37
NC_000005.8:g.131733264C>G NCBI36
NG_008982.1:g.4965C>G
NG_008982.2:g.4970C>G

Transcript Alleles

HGVS Amino-acid Change
NR_110997.1:n.73+171G>C