Canonical Allele Identifier: CA780892572
Gene: MIR3976HG HGNC NCBI

Linked Data

dbSNP Id: rs1450956712
MyVariant Identifiers: chr18:g.5856956C>G (hg19) chr18:g.5856957C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.5856957C>G , CM000680.2:g.5856957C>G GRCh38
NC_000018.9:g.5856956C>G , CM000680.1:g.5856956C>G GRCh37
NC_000018.8:g.5846956C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_172494.1:n.603-21486C>G
NR_172495.1:n.603-19296C>G
NR_172496.1:n.603-19296C>G
NR_172497.1:n.603-19296C>G
NR_172498.1:n.663-10156C>G
NR_172499.1:n.603-19296C>G
NR_172500.1:n.603-19296C>G
NR_172501.1:n.603-19296C>G
NR_172502.1:n.603-19296C>G
NR_172503.1:n.603-19296C>G
Search 100 bp 5'
Search 100 bp 3'