Canonical Allele Identifier: CA718346208
Gene: MIR193BHG HGNC NCBI

Linked Data

dbSNP Id: rs1339004926
MyVariant Identifiers: chr16:g.14395376C>T (hg19) chr16:g.14301519C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.14301519C>T , CM000678.2:g.14301519C>T GRCh38
NC_000016.9:g.14395376C>T , CM000678.1:g.14395376C>T GRCh37
NC_000016.8:g.14302877C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_170633.1:n.139C>T
Search 100 bp 5'
Search 100 bp 3'