Canonical Allele Identifier: CA2673162759

Gene: NSUN2

Linked Data

• gnomAD v4: 5-6619969-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.6619969T>G , CM000667.2:g.6619969T>G	GRCh38
NC_000005.9:g.6620082T>G , CM000667.1:g.6620082T>G	GRCh37
NC_000005.8:g.6673082T>G	NCBI36
NG_028215.1:g.18392A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264670.11:c.815+137A>C MANE Select	ENSP00000264670.6:n.815+137A>C
ENST00000264670.10:c.815+137A>C	ENSP00000264670.6:n.815+137A>C
ENST00000504374.5:c.*121+137A>C	ENSP00000421783.1:n.*121+137A>C
ENST00000505892.5:n.1384+137A>C
ENST00000506139.5:c.710+137A>C	ENSP00000420957.1:n.710+137A>C
NM_001193455.1:c.710+137A>C	NP_001180384.1:n.710+137A>C
NM_017755.5:c.815+137A>C	NP_060225.4:n.815+137A>C
NR_037947.1:n.1111+137A>C
NM_017755.6:c.815+137A>C MANE Select	NP_060225.4:n.815+137A>C
NM_001193455.2:c.710+137A>C	NP_001180384.1:n.710+137A>C
NR_037947.2:n.795+137A>C