Canonical Allele Identifier: CA562765049

Gene: MIR3936HG

Linked Data

• dbSNP Id: rs1001623575
• gnomAD v2: 5-131685990-T-C
• gnomAD v3: 5-132350297-T-C
• gnomAD v4: 5-132350297-T-C
• MyVariant Identifiers: chr5:g.131685990T>C (hg19) ; chr5:g.132350297T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132350297T>C , CM000667.2:g.132350297T>C	GRCh38
NC_000005.9:g.131685990T>C , CM000667.1:g.131685990T>C	GRCh37
NC_000005.8:g.131713889T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_110997.1:n.418-340A>G