Canonical Allele Identifier: CA127211558
Gene: MIR3936HG HGNC NCBI

Linked Data

dbSNP Id: rs1001623575
gnomAD v3: 5-132350297-T-G
gnomAD v4: 5-132350297-T-G
MyVariant Identifiers: chr5:g.131685990T>G (hg19) chr5:g.132350297T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132350297T>G , CM000667.2:g.132350297T>G GRCh38
NC_000005.9:g.131685990T>G , CM000667.1:g.131685990T>G GRCh37
NC_000005.8:g.131713889T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110997.1:n.418-340A>C
Search 100 bp 5'
Search 100 bp 3'