Canonical Allele Identifier: CA443101558
Gene: NSUN2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.6611184A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.6611071A>G , CM000667.2:g.6611071A>G GRCh38
NC_000005.9:g.6611184A>G , CM000667.1:g.6611184A>G GRCh37
NC_000005.8:g.6664184A>G NCBI36
NG_028215.1:g.27290T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264670.11:c.1110T>C MANE Select ENSP00000264670.6:p.Asp370=
ENST00000264670.10:c.1110T>C ENSP00000264670.6:p.Asp370=
ENST00000504374.5:c.*416T>C ENSP00000421783.1:n.*416T>C
ENST00000505892.5:n.1679T>C
ENST00000506139.5:c.1005T>C ENSP00000420957.1:p.Asp335=
NM_001193455.1:c.1005T>C NP_001180384.1:p.Asp335=
NM_017755.5:c.1110T>C NP_060225.4:p.Asp370=
NR_037947.1:n.1406T>C
NM_017755.6:c.1110T>C MANE Select NP_060225.4:p.Asp370=
NM_001193455.2:c.1005T>C NP_001180384.1:p.Asp335=
NR_037947.2:n.1090T>C