Canonical Allele Identifier: CA359121630
Gene: NSUN2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.6611191G>T (hg19) chr5:g.6611078G>T (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000264670.11:c.1103C>A MANE Select ENSP00000264670.6:p.Thr368Lys
ENST00000264670.10:c.1103C>A ENSP00000264670.6:p.Thr368Lys
ENST00000504374.5:c.*409C>A ENSP00000421783.1:n.*409C>A
ENST00000505892.5:n.1672C>A
ENST00000506139.5:c.998C>A ENSP00000420957.1:p.Thr333Lys
NM_001193455.1:c.998C>A NP_001180384.1:p.Thr333Lys
NM_017755.5:c.1103C>A NP_060225.4:p.Thr368Lys
NR_037947.1:n.1399C>A
NM_017755.6:c.1103C>A MANE Select NP_060225.4:p.Thr368Lys
NM_001193455.2:c.998C>A NP_001180384.1:p.Thr333Lys
NR_037947.2:n.1083C>A
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