Canonical Allele Identifier: CA803979874
Gene: MIR3936HG HGNC NCBI

Linked Data

dbSNP Id: rs1185157202
gnomAD v4: 5-132369586-T-G
MyVariant Identifiers: chr5:g.131705278T>G (hg19) chr5:g.132369586T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132369586T>G , CM000667.2:g.132369586T>G GRCh38
NC_000005.9:g.131705278T>G , CM000667.1:g.131705278T>G GRCh37
NC_000005.8:g.131733177T>G NCBI36
NG_008982.1:g.4878T>G
NG_008982.2:g.4883T>G

Transcript Alleles

HGVS Amino-acid Change
NR_110997.1:n.73+258A>C
Search 100 bp 5'
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