Canonical Allele Identifier: CA1525237843
Gene: NSUN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.6611069C= , CM000667.2:g.6611069C= GRCh38
NC_000005.9:g.6611182C= , CM000667.1:g.6611182C= GRCh37
NC_000005.8:g.6664182C= NCBI36
NG_028215.1:g.27292G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264670.11:c.1112G= MANE Select ENSP00000264670.6:p.Gly371=
ENST00000264670.10:c.1112G= ENSP00000264670.6:p.Gly371=
ENST00000504374.5:c.*418G= ENSP00000421783.1:n.*418G=
ENST00000505892.5:n.1681G=
ENST00000506139.5:c.1007G= ENSP00000420957.1:p.Gly336=
NM_001193455.1:c.1007G= NP_001180384.1:p.Gly336=
NM_017755.5:c.1112G= NP_060225.4:p.Gly371=
NR_037947.1:n.1408G=
NM_017755.6:c.1112G= MANE Select NP_060225.4:p.Gly371=
NM_001193455.2:c.1007G= NP_001180384.1:p.Gly336=
NR_037947.2:n.1092G=