Canonical Allele Identifier: CA803979947

Gene: MIR3936HG

Linked Data

• dbSNP Id: rs60978556
• MyVariant Identifiers: chr5:g.131705346C>G (hg19) ; chr5:g.132369654C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132369654C>G , CM000667.2:g.132369654C>G	GRCh38
NC_000005.9:g.131705346C>G , CM000667.1:g.131705346C>G	GRCh37
NC_000005.8:g.131733245C>G	NCBI36
NG_008982.1:g.4946C>G
NG_008982.2:g.4951C>G

Transcript Alleles

HGVS	Amino-acid Change
NR_110997.1:n.73+190G>C