Canonical Allele Identifier: CA803979842

Gene: MIR3936HG

Linked Data

• dbSNP Id: rs962696125
• MyVariant Identifiers: chr5:g.131705224T>G (hg19) ; chr5:g.132369532T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132369532T>G , CM000667.2:g.132369532T>G	GRCh38
NC_000005.9:g.131705224T>G , CM000667.1:g.131705224T>G	GRCh37
NC_000005.8:g.131733123T>G	NCBI36
NG_008982.1:g.4824T>G
NG_008982.2:g.4829T>G

Transcript Alleles

HGVS	Amino-acid Change
NR_110997.1:n.73+312A>C