Canonical Allele Identifier: CA1525237847
Gene: NSUN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.6611072T= , CM000667.2:g.6611072T= GRCh38
NC_000005.9:g.6611185T= , CM000667.1:g.6611185T= GRCh37
NC_000005.8:g.6664185T= NCBI36
NG_028215.1:g.27289A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264670.11:c.1109A= MANE Select ENSP00000264670.6:p.Asp370=
ENST00000264670.10:c.1109A= ENSP00000264670.6:p.Asp370=
ENST00000504374.5:c.*415A= ENSP00000421783.1:n.*415A=
ENST00000505892.5:n.1678A=
ENST00000506139.5:c.1004A= ENSP00000420957.1:p.Asp335=
NM_001193455.1:c.1004A= NP_001180384.1:p.Asp335=
NM_017755.5:c.1109A= NP_060225.4:p.Asp370=
NR_037947.1:n.1405A=
NM_017755.6:c.1109A= MANE Select NP_060225.4:p.Asp370=
NM_001193455.2:c.1004A= NP_001180384.1:p.Asp335=
NR_037947.2:n.1089A=