Canonical Allele Identifier: CA562767550

Gene: MIR3936HG

Linked Data

• dbSNP Id: rs1379527864
• gnomAD v2: 5-131705231-C-G
• gnomAD v3: 5-132369539-C-G
• gnomAD v4: 5-132369539-C-G
• MyVariant Identifiers: chr5:g.131705231C>G (hg19) ; chr5:g.132369539C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132369539C>G , CM000667.2:g.132369539C>G	GRCh38
NC_000005.9:g.131705231C>G , CM000667.1:g.131705231C>G	GRCh37
NC_000005.8:g.131733130C>G	NCBI36
NG_008982.1:g.4831C>G
NG_008982.2:g.4836C>G

Transcript Alleles

HGVS	Amino-acid Change
NR_110997.1:n.73+305G>C