Canonical Allele Identifier: CA1525232511
Gene: NSUN2 HGNC NCBI

Linked Data

dbSNP Id: rs1737366936
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.6619933T>G , CM000667.2:g.6619933T>G GRCh38
NC_000005.9:g.6620046T>G , CM000667.1:g.6620046T>G GRCh37
NC_000005.8:g.6673046T>G NCBI36
NG_028215.1:g.18428A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264670.11:c.815+173A>C MANE Select ENSP00000264670.6:n.815+173A>C
ENST00000264670.10:c.815+173A>C ENSP00000264670.6:n.815+173A>C
ENST00000504374.5:c.*121+173A>C ENSP00000421783.1:n.*121+173A>C
ENST00000505892.5:n.1384+173A>C
ENST00000506139.5:c.710+173A>C ENSP00000420957.1:n.710+173A>C
NM_001193455.1:c.710+173A>C NP_001180384.1:n.710+173A>C
NM_017755.5:c.815+173A>C NP_060225.4:n.815+173A>C
NR_037947.1:n.1111+173A>C
NM_017755.6:c.815+173A>C MANE Select NP_060225.4:n.815+173A>C
NM_001193455.2:c.710+173A>C NP_001180384.1:n.710+173A>C
NR_037947.2:n.795+173A>C
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