Canonical Allele Identifier: CA127195717

Gene: MIR3936HG

Linked Data

• dbSNP Id: rs1033802535
• gnomAD v3: 5-132369644-A-G
• gnomAD v4: 5-132369644-A-G
• MyVariant Identifiers: chr5:g.131705336A>G (hg19) ; chr5:g.132369644A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132369644A>G , CM000667.2:g.132369644A>G	GRCh38
NC_000005.9:g.131705336A>G , CM000667.1:g.131705336A>G	GRCh37
NC_000005.8:g.131733235A>G	NCBI36
NG_008982.1:g.4936A>G
NG_008982.2:g.4941A>G

Transcript Alleles

HGVS	Amino-acid Change
NR_110997.1:n.73+200T>C