Canonical Allele Identifier: CA1525232517

Gene: NSUN2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.6619940T= , CM000667.2:g.6619940T=	GRCh38
NC_000005.9:g.6620053T= , CM000667.1:g.6620053T=	GRCh37
NC_000005.8:g.6673053T=	NCBI36
NG_028215.1:g.18421A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264670.11:c.815+166A= MANE Select	ENSP00000264670.6:n.815+166A=
ENST00000264670.10:c.815+166A=	ENSP00000264670.6:n.815+166A=
ENST00000504374.5:c.*121+166A=	ENSP00000421783.1:n.*121+166A=
ENST00000505892.5:n.1384+166A=
ENST00000506139.5:c.710+166A=	ENSP00000420957.1:n.710+166A=
NM_001193455.1:c.710+166A=	NP_001180384.1:n.710+166A=
NM_017755.5:c.815+166A=	NP_060225.4:n.815+166A=
NR_037947.1:n.1111+166A=
NM_017755.6:c.815+166A= MANE Select	NP_060225.4:n.815+166A=
NM_001193455.2:c.710+166A=	NP_001180384.1:n.710+166A=
NR_037947.2:n.795+166A=