Canonical Allele Identifier: CA174644

Gene: NETO2

Linked Data

• ClinVar Variation Id: 161712
• ClinVar RCV Id: RCV000149248
• dbSNP Id: rs193920943
• COSMIC: COSM1178710
• MyVariant Identifiers: chr16:g.47117178C>G (hg19) ; chr16:g.47083267C>G (hg38)
• PubMed: PMID:23265383

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.47083267C>G , CM000678.2:g.47083267C>G	GRCh38
NC_000016.9:g.47117178C>G , CM000678.1:g.47117178C>G	GRCh37
NC_000016.8:g.45674679C>G	NCBI36
NG_047201.1:g.65759G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000562435.6:c.1532G>C MANE Select	ENSP00000455169.1:p.Arg511Thr
ENST00000303155.9:c.1511G>C	ENSP00000306726.5:p.Arg504Thr
ENST00000562435.5:c.1532G>C	ENSP00000455169.1:p.Arg511Thr
ENST00000562559.5:c.1050G>C
ENST00000564667.1:c.639G>C
NM_001201477.1:c.1511G>C	NP_001188406.1:p.Arg504Thr
NM_018092.4:c.1532G>C	NP_060562.3:p.Arg511Thr
XM_006721289.1:c.1418G>C	XP_006721352.1:p.Arg473Thr
XM_006721291.1:c.1397G>C	XP_006721354.1:p.Arg466Thr
XM_017023740.1:c.1124G>C	XP_016879229.1:p.Arg375Thr
NM_001201477.2:c.1511G>C	NP_001188406.1:p.Arg504Thr
NM_018092.5:c.1532G>C MANE Select	NP_060562.3:p.Arg511Thr