Canonical Allele Identifier: CA1081635037
Gene: MIR3936HG HGNC NCBI

Linked Data

dbSNP Id: rs1751796120
gnomAD v3: 5-132369636-C-G
gnomAD v4: 5-132369636-C-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132369636C>G , CM000667.2:g.132369636C>G GRCh38
NC_000005.9:g.131705328C>G , CM000667.1:g.131705328C>G GRCh37
NC_000005.8:g.131733227C>G NCBI36
NG_008982.1:g.4928C>G
NG_008982.2:g.4933C>G

Transcript Alleles

HGVS Amino-acid Change
NR_110997.1:n.73+208G>C
Search 100 bp 5'
Search 100 bp 3'