Canonical Allele Identifier: CA803979954
Gene: MIR3936HG HGNC NCBI

Linked Data

dbSNP Id: rs1392067290
gnomAD v3: 5-132369669-C-T
gnomAD v4: 5-132369669-C-T
MyVariant Identifiers: chr5:g.131705361C>T (hg19) chr5:g.132369669C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132369669C>T , CM000667.2:g.132369669C>T GRCh38
NC_000005.9:g.131705361C>T , CM000667.1:g.131705361C>T GRCh37
NC_000005.8:g.131733260C>T NCBI36
NG_008982.1:g.4961C>T
NG_008982.2:g.4966C>T

Transcript Alleles

HGVS Amino-acid change
NR_110997.1:n.73+175G>A
Search 100 bp 5'
Search 100 bp 3'