Canonical Allele Identifier: CA803979923

Gene: MIR3936HG

Linked Data

• dbSNP Id: rs937799028
• MyVariant Identifiers: chr5:g.131705313G>C (hg19) ; chr5:g.132369621G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132369621G>C , CM000667.2:g.132369621G>C	GRCh38
NC_000005.9:g.131705313G>C , CM000667.1:g.131705313G>C	GRCh37
NC_000005.8:g.131733212G>C	NCBI36
NG_008982.1:g.4913G>C
NG_008982.2:g.4918G>C

Transcript Alleles

HGVS	Amino-acid Change
NR_110997.1:n.73+223C>G