Canonical Allele Identifier: CA127195598
Gene: MIR3936HG HGNC NCBI

Linked Data

dbSNP Id: rs768079676
gnomAD v3: 5-132369542-A-G
gnomAD v4: 5-132369542-A-G
MyVariant Identifiers: chr5:g.131705234A>G (hg19) chr5:g.132369542A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132369542A>G , CM000667.2:g.132369542A>G GRCh38
NC_000005.9:g.131705234A>G , CM000667.1:g.131705234A>G GRCh37
NC_000005.8:g.131733133A>G NCBI36
NG_008982.1:g.4834A>G
NG_008982.2:g.4839A>G

Transcript Alleles

HGVS Amino-acid Change
NR_110997.1:n.73+302T>C
Search 100 bp 5'
Search 100 bp 3'