Canonical Allele Identifier: CA562767549
Gene: MIR3936HG HGNC NCBI

Linked Data

dbSNP Id: rs1174225128
gnomAD v2: 5-131705225-C-T
gnomAD v3: 5-132369533-C-T
gnomAD v4: 5-132369533-C-T
MyVariant Identifiers: chr5:g.131705225C>T (hg19) chr5:g.132369533C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132369533C>T , CM000667.2:g.132369533C>T GRCh38
NC_000005.9:g.131705225C>T , CM000667.1:g.131705225C>T GRCh37
NC_000005.8:g.131733124C>T NCBI36
NG_008982.1:g.4825C>T
NG_008982.2:g.4830C>T

Transcript Alleles

HGVS Amino-acid Change
NR_110997.1:n.73+311G>A
Search 100 bp 5'
Search 100 bp 3'