Canonical Allele Identifier: CA1583129111
Gene: MIR3936HG HGNC NCBI

Linked Data

dbSNP Id: rs1751413992
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132350307C>A , CM000667.2:g.132350307C>A GRCh38
NC_000005.9:g.131686000C>A , CM000667.1:g.131686000C>A GRCh37
NC_000005.8:g.131713899C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110997.1:n.418-350G>T
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