Canonical Allele Identifier: CA1583137298
Gene: MIR3936HG HGNC NCBI

Linked Data

dbSNP Id: rs933841311
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132369534G>C , CM000667.2:g.132369534G>C GRCh38
NC_000005.9:g.131705226G>C , CM000667.1:g.131705226G>C GRCh37
NC_000005.8:g.131733125G>C NCBI36
NG_008982.1:g.4826G>C
NG_008982.2:g.4831G>C

Transcript Alleles

HGVS Amino-acid Change
NR_110997.1:n.73+310C>G
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