Canonical Allele Identifier: CA2673162848

Gene: NSUN2

Linked Data

• gnomAD v4: 5-6619987-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.6619987T>A , CM000667.2:g.6619987T>A	GRCh38
NC_000005.9:g.6620100T>A , CM000667.1:g.6620100T>A	GRCh37
NC_000005.8:g.6673100T>A	NCBI36
NG_028215.1:g.18374A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264670.11:c.815+119A>T MANE Select	ENSP00000264670.6:n.815+119A>T
ENST00000264670.10:c.815+119A>T	ENSP00000264670.6:n.815+119A>T
ENST00000504374.5:c.*121+119A>T	ENSP00000421783.1:n.*121+119A>T
ENST00000505892.5:n.1384+119A>T
ENST00000506139.5:c.710+119A>T	ENSP00000420957.1:n.710+119A>T
NM_001193455.1:c.710+119A>T	NP_001180384.1:n.710+119A>T
NM_017755.5:c.815+119A>T	NP_060225.4:n.815+119A>T
NR_037947.1:n.1111+119A>T
NM_017755.6:c.815+119A>T MANE Select	NP_060225.4:n.815+119A>T
NM_001193455.2:c.710+119A>T	NP_001180384.1:n.710+119A>T
NR_037947.2:n.795+119A>T