Canonical Allele Identifier: CA295688498
Gene: MIR3976HG HGNC NCBI

Linked Data

dbSNP Id: rs1048758671
gnomAD v3: 18-5856912-C-G
gnomAD v4: 18-5856912-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.5856912C>G , CM000680.2:g.5856912C>G GRCh38
NC_000018.9:g.5856911C>G , CM000680.1:g.5856911C>G GRCh37
NC_000018.8:g.5846911C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_172494.1:n.603-21531C>G
NR_172495.1:n.603-19341C>G
NR_172496.1:n.603-19341C>G
NR_172497.1:n.603-19341C>G
NR_172498.1:n.663-10201C>G
NR_172499.1:n.603-19341C>G
NR_172500.1:n.603-19341C>G
NR_172501.1:n.603-19341C>G
NR_172502.1:n.603-19341C>G
NR_172503.1:n.603-19341C>G