Canonical Allele Identifier: CA987452965
Gene: MIR3976HG HGNC NCBI

Linked Data

dbSNP Id: rs2095145579
gnomAD v3: 18-5856906-G-A
gnomAD v4: 18-5856906-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.5856906G>A , CM000680.2:g.5856906G>A GRCh38
NC_000018.9:g.5856905G>A , CM000680.1:g.5856905G>A GRCh37
NC_000018.8:g.5846905G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_172494.1:n.603-21537G>A
NR_172495.1:n.603-19347G>A
NR_172496.1:n.603-19347G>A
NR_172497.1:n.603-19347G>A
NR_172498.1:n.663-10207G>A
NR_172499.1:n.603-19347G>A
NR_172500.1:n.603-19347G>A
NR_172501.1:n.603-19347G>A
NR_172502.1:n.603-19347G>A
NR_172503.1:n.603-19347G>A
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