Canonical Allele Identifier: CA974004109
Gene: ROGDI HGNC NCBI

Linked Data

dbSNP Id: rs577019256
gnomAD v3: 16-4798254-G-C
gnomAD v4: 16-4798254-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.4798254G>C , CM000678.2:g.4798254G>C GRCh38
NC_000016.9:g.4848255G>C , CM000678.1:g.4848255G>C GRCh37
NC_000016.8:g.4788256G>C NCBI36
NG_032174.1:g.9697C>G , LRG_455:g.9697C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000322048.12:c.532-70C>G MANE Select ENSP00000322832.6:n.532-70C>G
ENST00000322048.11:c.532-70C>G ENSP00000322832.5:n.532-70C>G
ENST00000586153.1:c.178-70C>G ENSP00000464699.1:n.178-70C>G
ENST00000586336.5:n.631-70C>G
ENST00000586504.5:c.312-70C>G
ENST00000587377.5:c.545-70C>G ENSP00000468343.1:n.545-70C>G
ENST00000587711.5:c.217-70C>G ENSP00000467459.1:n.217-70C>G
ENST00000587843.5:c.*270-70C>G ENSP00000465970.1:n.*270-70C>G
ENST00000588201.5:c.*523-70C>G ENSP00000466529.1:n.*523-70C>G
ENST00000589543.5:n.489-70C>G
ENST00000591292.5:n.1861-70C>G
ENST00000591392.5:c.460-70C>G ENSP00000467509.1:n.460-70C>G
ENST00000592019.1:c.77-439C>G
NM_024589.2:c.532-70C>G , LRG_455t1:c.532-70C>G NP_078865.1:n.532-70C>G
NR_046480.1:n.856-70C>G
XM_006720947.2:c.532-70C>G XP_006721010.1:n.532-70C>G
XM_006720948.2:c.262-70C>G XP_006721011.1:n.262-70C>G
XM_006720947.4:c.532-70C>G XP_006721010.1:n.532-70C>G
XM_006720948.4:c.262-70C>G XP_006721011.1:n.262-70C>G
NM_024589.3:c.532-70C>G MANE Select NP_078865.1:n.532-70C>G
NR_046480.2:n.539-70C>G