Canonical Allele Identifier: CA359121617
Gene: NSUN2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.6611187T>G (hg19) chr5:g.6611074T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.6611074T>G , CM000667.2:g.6611074T>G GRCh38
NC_000005.9:g.6611187T>G , CM000667.1:g.6611187T>G GRCh37
NC_000005.8:g.6664187T>G NCBI36
NG_028215.1:g.27287A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000264670.11:c.1107A>C MANE Select ENSP00000264670.6:p.Lys369Asn
ENST00000264670.10:c.1107A>C ENSP00000264670.6:p.Lys369Asn
ENST00000504374.5:c.*413A>C ENSP00000421783.1:n.*413A>C
ENST00000505892.5:n.1676A>C
ENST00000506139.5:c.1002A>C ENSP00000420957.1:p.Lys334Asn
NM_001193455.1:c.1002A>C NP_001180384.1:p.Lys334Asn
NM_017755.5:c.1107A>C NP_060225.4:p.Lys369Asn
NR_037947.1:n.1403A>C
NM_017755.6:c.1107A>C MANE Select NP_060225.4:p.Lys369Asn
NM_001193455.2:c.1002A>C NP_001180384.1:p.Lys334Asn
NR_037947.2:n.1087A>C
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