Canonical Allele Identifier: CA359121629
Gene: NSUN2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.6611078G>C , CM000667.2:g.6611078G>C GRCh38
NC_000005.9:g.6611191G>C , CM000667.1:g.6611191G>C GRCh37
NC_000005.8:g.6664191G>C NCBI36
NG_028215.1:g.27283C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264670.11:c.1103C>G MANE Select ENSP00000264670.6:p.Thr368Arg
ENST00000264670.10:c.1103C>G ENSP00000264670.6:p.Thr368Arg
ENST00000504374.5:c.*409C>G ENSP00000421783.1:n.*409C>G
ENST00000505892.5:n.1672C>G
ENST00000506139.5:c.998C>G ENSP00000420957.1:p.Thr333Arg
NM_001193455.1:c.998C>G NP_001180384.1:p.Thr333Arg
NM_017755.5:c.1103C>G NP_060225.4:p.Thr368Arg
NR_037947.1:n.1399C>G
NM_017755.6:c.1103C>G MANE Select NP_060225.4:p.Thr368Arg
NM_001193455.2:c.998C>G NP_001180384.1:p.Thr333Arg
NR_037947.2:n.1083C>G