Canonical Allele Identifier: CA1525237855
Gene: NSUN2 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000264670.11:c.1103C= MANE Select ENSP00000264670.6:p.Thr368=
ENST00000264670.10:c.1103C= ENSP00000264670.6:p.Thr368=
ENST00000504374.5:c.*409C= ENSP00000421783.1:n.*409C=
ENST00000505892.5:n.1672C=
ENST00000506139.5:c.998C= ENSP00000420957.1:p.Thr333=
NM_001193455.1:c.998C= NP_001180384.1:p.Thr333=
NM_017755.5:c.1103C= NP_060225.4:p.Thr368=
NR_037947.1:n.1399C=
NM_017755.6:c.1103C= MANE Select NP_060225.4:p.Thr368=
NM_001193455.2:c.998C= NP_001180384.1:p.Thr333=
NR_037947.2:n.1083C=