Canonical Allele Identifier: CA359121639
Gene: NSUN2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.6611192T>C (hg19) chr5:g.6611079T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.6611079T>C , CM000667.2:g.6611079T>C GRCh38
NC_000005.9:g.6611192T>C , CM000667.1:g.6611192T>C GRCh37
NC_000005.8:g.6664192T>C NCBI36
NG_028215.1:g.27282A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264670.11:c.1102A>G MANE Select ENSP00000264670.6:p.Thr368Ala
ENST00000264670.10:c.1102A>G ENSP00000264670.6:p.Thr368Ala
ENST00000504374.5:c.*408A>G ENSP00000421783.1:n.*408A>G
ENST00000505892.5:n.1671A>G
ENST00000506139.5:c.997A>G ENSP00000420957.1:p.Thr333Ala
NM_001193455.1:c.997A>G NP_001180384.1:p.Thr333Ala
NM_017755.5:c.1102A>G NP_060225.4:p.Thr368Ala
NR_037947.1:n.1398A>G
NM_017755.6:c.1102A>G MANE Select NP_060225.4:p.Thr368Ala
NM_001193455.2:c.997A>G NP_001180384.1:p.Thr333Ala
NR_037947.2:n.1082A>G
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