Canonical Allele Identifier: CA1525232498
Gene: NSUN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.6619931G= , CM000667.2:g.6619931G= GRCh38
NC_000005.9:g.6620044G= , CM000667.1:g.6620044G= GRCh37
NC_000005.8:g.6673044G= NCBI36
NG_028215.1:g.18430C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264670.11:c.815+175C= MANE Select ENSP00000264670.6:n.815+175C=
ENST00000264670.10:c.815+175C= ENSP00000264670.6:n.815+175C=
ENST00000504374.5:c.*121+175C= ENSP00000421783.1:n.*121+175C=
ENST00000505892.5:n.1384+175C=
ENST00000506139.5:c.710+175C= ENSP00000420957.1:n.710+175C=
NM_001193455.1:c.710+175C= NP_001180384.1:n.710+175C=
NM_017755.5:c.815+175C= NP_060225.4:n.815+175C=
NR_037947.1:n.1111+175C=
NM_017755.6:c.815+175C= MANE Select NP_060225.4:n.815+175C=
NM_001193455.2:c.710+175C= NP_001180384.1:n.710+175C=
NR_037947.2:n.795+175C=