Canonical Allele Identifier: CA803979845
Gene: MIR3936HG HGNC NCBI

Linked Data

dbSNP Id: rs1222377526
gnomAD v3: 5-132369535-G-T
gnomAD v4: 5-132369535-G-T
MyVariant Identifiers: chr5:g.131705227G>T (hg19) chr5:g.132369535G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132369535G>T , CM000667.2:g.132369535G>T GRCh38
NC_000005.9:g.131705227G>T , CM000667.1:g.131705227G>T GRCh37
NC_000005.8:g.131733126G>T NCBI36
NG_008982.1:g.4827G>T
NG_008982.2:g.4832G>T

Transcript Alleles

HGVS Amino-acid Change
NR_110997.1:n.73+309C>A
Search 100 bp 5'
Search 100 bp 3'