Canonical Allele Identifier: CA127195738
Gene: MIR3936HG HGNC NCBI

Linked Data

dbSNP Id: rs998754700
gnomAD v2: 5-131705375-C-G
gnomAD v3: 5-132369683-C-G
gnomAD v4: 5-132369683-C-G
MyVariant Identifiers: chr5:g.131705375C>G (hg19) chr5:g.132369683C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132369683C>G , CM000667.2:g.132369683C>G GRCh38
NC_000005.9:g.131705375C>G , CM000667.1:g.131705375C>G GRCh37
NC_000005.8:g.131733274C>G NCBI36
NG_008982.1:g.4975C>G
NG_008982.2:g.4980C>G

Transcript Alleles

HGVS Amino-acid Change
NR_110997.1:n.73+161G>C
Search 100 bp 5'
Search 100 bp 3'