Canonical Allele Identifier: CA770821437

Gene: MIR4432HG

Linked Data

• dbSNP Id: rs1259809580
• MyVariant Identifiers: chr2:g.60608794A>G (hg19) ; chr2:g.60381659A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.60381659A>G , CM000664.2:g.60381659A>G	GRCh38
NC_000002.11:g.60608794A>G , CM000664.1:g.60608794A>G	GRCh37
NC_000002.10:g.60462298A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_132991.1:n.93+1285T>C
NR_132992.1:n.70+9647T>C