Canonical Allele Identifier: CA295688631

Gene: MIR3976HG

Linked Data

• dbSNP Id: rs770202022
• MyVariant Identifiers: chr18:g.5857246T>C (hg19) ; chr18:g.5857247T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.5857247T>C , CM000680.2:g.5857247T>C	GRCh38
NC_000018.9:g.5857246T>C , CM000680.1:g.5857246T>C	GRCh37
NC_000018.8:g.5847246T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_172494.1:n.603-21196T>C
NR_172495.1:n.603-19006T>C
NR_172496.1:n.603-19006T>C
NR_172497.1:n.603-19006T>C
NR_172498.1:n.663-9866T>C
NR_172499.1:n.603-19006T>C
NR_172500.1:n.603-19006T>C
NR_172501.1:n.603-19006T>C
NR_172502.1:n.603-19006T>C
NR_172503.1:n.603-19006T>C