Canonical Allele Identifier: CA1583129152
Gene: MIR3936HG HGNC NCBI

Linked Data

dbSNP Id: rs1561553619

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132350418T>C , CM000667.2:g.132350418T>C GRCh38
NC_000005.9:g.131686111T>C , CM000667.1:g.131686111T>C GRCh37
NC_000005.8:g.131714010T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110997.1:n.418-461A>G