Canonical Allele Identifier: CA2673162699

Gene: NSUN2

Linked Data

• gnomAD v4: 5-6619955-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.6619955T>A , CM000667.2:g.6619955T>A	GRCh38
NC_000005.9:g.6620068T>A , CM000667.1:g.6620068T>A	GRCh37
NC_000005.8:g.6673068T>A	NCBI36
NG_028215.1:g.18406A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264670.11:c.815+151A>T MANE Select	ENSP00000264670.6:n.815+151A>T
ENST00000264670.10:c.815+151A>T	ENSP00000264670.6:n.815+151A>T
ENST00000504374.5:c.*121+151A>T	ENSP00000421783.1:n.*121+151A>T
ENST00000505892.5:n.1384+151A>T
ENST00000506139.5:c.710+151A>T	ENSP00000420957.1:n.710+151A>T
NM_001193455.1:c.710+151A>T	NP_001180384.1:n.710+151A>T
NM_017755.5:c.815+151A>T	NP_060225.4:n.815+151A>T
NR_037947.1:n.1111+151A>T
NM_017755.6:c.815+151A>T MANE Select	NP_060225.4:n.815+151A>T
NM_001193455.2:c.710+151A>T	NP_001180384.1:n.710+151A>T
NR_037947.2:n.795+151A>T