Canonical Allele Identifier: CA803979868
Gene: MIR3936HG HGNC NCBI

Linked Data

dbSNP Id: rs1176836656
gnomAD v3: 5-132369575-C-G
gnomAD v4: 5-132369575-C-G
MyVariant Identifiers: chr5:g.131705267C>G (hg19) chr5:g.132369575C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132369575C>G , CM000667.2:g.132369575C>G GRCh38
NC_000005.9:g.131705267C>G , CM000667.1:g.131705267C>G GRCh37
NC_000005.8:g.131733166C>G NCBI36
NG_008982.1:g.4867C>G
NG_008982.2:g.4872C>G

Transcript Alleles

HGVS Amino-acid Change
NR_110997.1:n.73+269G>C
Search 100 bp 5'
Search 100 bp 3'