Canonical Allele Identifier: CA1525232582
Gene: NSUN2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.6619974G= , CM000667.2:g.6619974G= GRCh38
NC_000005.9:g.6620087G= , CM000667.1:g.6620087G= GRCh37
NC_000005.8:g.6673087G= NCBI36
NG_028215.1:g.18387C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264670.11:c.815+132C= MANE Select ENSP00000264670.6:n.815+132C=
ENST00000264670.10:c.815+132C= ENSP00000264670.6:n.815+132C=
ENST00000504374.5:c.*121+132C= ENSP00000421783.1:n.*121+132C=
ENST00000505892.5:n.1384+132C=
ENST00000506139.5:c.710+132C= ENSP00000420957.1:n.710+132C=
NM_001193455.1:c.710+132C= NP_001180384.1:n.710+132C=
NM_017755.5:c.815+132C= NP_060225.4:n.815+132C=
NR_037947.1:n.1111+132C=
NM_017755.6:c.815+132C= MANE Select NP_060225.4:n.815+132C=
NM_001193455.2:c.710+132C= NP_001180384.1:n.710+132C=
NR_037947.2:n.795+132C=
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