Canonical Allele Identifier: CA12063679
Gene: MIR3936HG HGNC NCBI

Linked Data

ClinVar Variation Id: 1266598
ClinVar RCV Id: RCV001676421
dbSNP Id: rs2631368
gnomAD v2: 5-131705297-T-G
gnomAD v3: 5-132369605-T-G
gnomAD v4: 5-132369605-T-G
MyVariant Identifiers: chr5:g.131705297T>G (hg19) chr5:g.132369605T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132369605T>G , CM000667.2:g.132369605T>G GRCh38
NC_000005.9:g.131705297T>G , CM000667.1:g.131705297T>G GRCh37
NC_000005.8:g.131733196T>G NCBI36
NG_008982.1:g.4897T>G
NG_008982.2:g.4902T>G

Transcript Alleles

HGVS Amino-acid Change
NR_110997.1:n.73+239A>C
Search 100 bp 5'
Search 100 bp 3'