Canonical Allele Identifier: CA7882740

Gene: ROGDI

Linked Data

• dbSNP Id: rs538455657
• ExAC: 16:4849679 C / G
• gnomAD v2: 16-4849679-C-G
• gnomAD v3: 16-4799678-C-G
• gnomAD v4: 16-4799678-C-G
• MyVariant Identifiers: chr16:g.4849679C>G (hg19) ; chr16:g.4799678C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4799678C>G , CM000678.2:g.4799678C>G	GRCh38
NC_000016.9:g.4849679C>G , CM000678.1:g.4849679C>G	GRCh37
NC_000016.8:g.4789680C>G	NCBI36
NG_032174.1:g.8273G>C , LRG_455:g.8273G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.432+8G>C MANE Select	ENSP00000322832.6:n.432+8G>C
ENST00000322048.11:c.432+8G>C	ENSP00000322832.5:n.432+8G>C
ENST00000585653.1:n.564+8G>C
ENST00000586153.1:c.177+8G>C	ENSP00000464699.1:n.177+8G>C
ENST00000586336.5:n.531+8G>C
ENST00000586504.5:c.212+8G>C
ENST00000587377.5:c.423+17G>C	ENSP00000468343.1:n.423+17G>C
ENST00000587711.5:c.118-1011G>C	ENSP00000467459.1:n.118-1011G>C
ENST00000587843.5:c.*170+8G>C	ENSP00000465970.1:n.*170+8G>C
ENST00000588201.5:c.*289+8G>C	ENSP00000466529.1:n.*289+8G>C
ENST00000589543.5:n.389+8G>C
ENST00000591292.5:n.1761+8G>C
ENST00000591392.5:c.360+8G>C	ENSP00000467509.1:n.360+8G>C
ENST00000592019.1:c.76+83G>C
NM_024589.2:c.432+8G>C , LRG_455t1:c.432+8G>C	NP_078865.1:n.432+8G>C
NR_046480.1:n.756+8G>C
XM_006720947.2:c.432+8G>C	XP_006721010.1:n.432+8G>C
XM_006720948.2:c.162+8G>C	XP_006721011.1:n.162+8G>C
XM_006720947.4:c.432+8G>C	XP_006721010.1:n.432+8G>C
XM_006720948.4:c.162+8G>C	XP_006721011.1:n.162+8G>C
NM_024589.3:c.432+8G>C MANE Select	NP_078865.1:n.432+8G>C
NR_046480.2:n.439+8G>C