Canonical Allele Identifier: CA2710221557
Gene: MIR3936HG HGNC NCBI

Linked Data

dbSNP Id: rs2126753472
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132350267G>A , CM000667.2:g.132350267G>A GRCh38
NC_000005.9:g.131685960G>A , CM000667.1:g.131685960G>A GRCh37
NC_000005.8:g.131713859G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110997.1:n.418-310C>T
Search 100 bp 5'
Search 100 bp 3'