Canonical Allele Identifier: CA1583129092
Gene: MIR3936HG HGNC NCBI

Linked Data

dbSNP Id: rs1580857123

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132350266A>G , CM000667.2:g.132350266A>G GRCh38
NC_000005.9:g.131685959A>G , CM000667.1:g.131685959A>G GRCh37
NC_000005.8:g.131713858A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110997.1:n.418-309T>C