Canonical Allele Identifier: CA822246640

Gene: RNASET2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.166956254G>C , CM000668.2:g.166956254G>C	GRCh38
NC_000006.11:g.167369742G>C , CM000668.1:g.167369742G>C	GRCh37
NC_000006.10:g.167289732G>C	NCBI36
NG_016280.1:g.5336C>G
NG_016280.2:g.5336C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_003730.6:c.-72C>G MANE Select	NP_003721.2:n.-72C>G
ENST00000508775.6:c.-72C>G MANE Select	ENSP00000426455.2:n.-72C>G
NM_003730.4:c.-72C>G	NP_003721.2:n.-72C>G
NM_003730.5:c.-72C>G	NP_003721.2:n.-72C>G
ENST00000028008.9:c.-72C>G	ENSP00000028008.5:n.-72C>G
ENST00000358165.7:n.243+695C>G
ENST00000366855.10:c.-319C>G	ENSP00000424947.1:n.-319C>G
ENST00000421787.5:c.-72C>G	ENSP00000390833.1:n.-72C>G
ENST00000476238.6:c.-9-63C>G	ENSP00000422846.1:n.-9-63C>G
ENST00000478180.6:c.-9-63C>G	ENSP00000426059.1:n.-9-63C>G
ENST00000508775.5:c.-72C>G	ENSP00000426455.1:n.-72C>G
ENST00000611959.1:c.-72C>G	ENSP00000480244.1:n.-72C>G
ENST00000611959.2:c.-72C>G	ENSP00000480244.2:n.-72C>G
ENST00000620173.4:c.-72C>G	ENSP00000482755.1:n.-72C>G
ENST00000620173.5:c.-72C>G	ENSP00000482755.2:n.-72C>G
ENST00000683333.1:n.314C>G
ENST00000683770.1:c.-72C>G	ENSP00000507710.1:n.-72C>G
XM_017011398.1:c.-292C>G	XP_016866887.1:n.-292C>G
XM_017011399.1:c.-72C>G	XP_016866888.1:n.-72C>G
XM_024446575.1:c.-453C>G	XP_024302343.1:n.-453C>G