Canonical Allele Identifier: CA127211568
Gene: MIR3936HG HGNC NCBI

Linked Data

dbSNP Id: rs573695197
gnomAD v2: 5-131686020-A-C
gnomAD v3: 5-132350327-A-C
gnomAD v4: 5-132350327-A-C
MyVariant Identifiers: chr5:g.131686020A>C (hg19) chr5:g.132350327A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132350327A>C , CM000667.2:g.132350327A>C GRCh38
NC_000005.9:g.131686020A>C , CM000667.1:g.131686020A>C GRCh37
NC_000005.8:g.131713919A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110997.1:n.418-370T>G
Search 100 bp 5'
Search 100 bp 3'