Canonical Allele Identifier: CA7882780

Gene: ROGDI

Linked Data

• dbSNP Id: rs371786783
• ExAC: 16:4849816 A / G
• gnomAD v2: 16-4849816-A-G
• gnomAD v3: 16-4799815-A-G
• gnomAD v4: 16-4799815-A-G
• MyVariant Identifiers: chr16:g.4849816A>G (hg19) ; chr16:g.4799815A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4799815A>G , CM000678.2:g.4799815A>G	GRCh38
NC_000016.9:g.4849816A>G , CM000678.1:g.4849816A>G	GRCh37
NC_000016.8:g.4789817A>G	NCBI36
NG_032174.1:g.8136T>C , LRG_455:g.8136T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.337-34T>C MANE Select	ENSP00000322832.6:n.337-34T>C
ENST00000322048.11:c.337-34T>C	ENSP00000322832.5:n.337-34T>C
ENST00000585653.1:n.469-34T>C
ENST00000586153.1:c.82-34T>C	ENSP00000464699.1:n.82-34T>C
ENST00000586336.5:n.436-34T>C
ENST00000586504.5:c.117-34T>C
ENST00000587377.5:c.337-34T>C	ENSP00000468343.1:n.337-34T>C
ENST00000587711.5:c.118-1148T>C	ENSP00000467459.1:n.118-1148T>C
ENST00000587843.5:c.*75-34T>C	ENSP00000465970.1:n.*75-34T>C
ENST00000588201.5:c.*194-34T>C	ENSP00000466529.1:n.*194-34T>C
ENST00000589543.5:n.294-34T>C
ENST00000591292.5:n.1666-34T>C
ENST00000591392.5:c.265-34T>C	ENSP00000467509.1:n.265-34T>C
ENST00000592019.1:c.56-34T>C
NM_024589.2:c.337-34T>C , LRG_455t1:c.337-34T>C	NP_078865.1:n.337-34T>C
NR_046480.1:n.661-34T>C
XM_006720947.2:c.337-34T>C	XP_006721010.1:n.337-34T>C
XM_006720948.2:c.67-34T>C	XP_006721011.1:n.67-34T>C
XM_006720947.4:c.337-34T>C	XP_006721010.1:n.337-34T>C
XM_006720948.4:c.67-34T>C	XP_006721011.1:n.67-34T>C
NM_024589.3:c.337-34T>C MANE Select	NP_078865.1:n.337-34T>C
NR_046480.2:n.344-34T>C