Canonical Allele Identifier: CA127195577

Gene: MIR3936HG

Linked Data

• dbSNP Id: rs914901811
• gnomAD v3: 5-132369515-G-C
• gnomAD v4: 5-132369515-G-C
• MyVariant Identifiers: chr5:g.131705207G>C (hg19) ; chr5:g.132369515G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132369515G>C , CM000667.2:g.132369515G>C	GRCh38
NC_000005.9:g.131705207G>C , CM000667.1:g.131705207G>C	GRCh37
NC_000005.8:g.131733106G>C	NCBI36
NG_008982.1:g.4807G>C
NG_008982.2:g.4812G>C

Transcript Alleles

HGVS	Amino-acid Change
NR_110997.1:n.73+329C>G