Canonical Allele Identifier: CA530540448

Gene: ODC1

Linked Data

• dbSNP Id: rs1250572225
• gnomAD v2: 2-10588038-A-G
• gnomAD v3: 2-10447912-A-G
• gnomAD v4: 2-10447912-A-G
• MyVariant Identifiers: chr2:g.10588038A>G (hg19) ; chr2:g.10447912A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.10447912A>G , CM000664.2:g.10447912A>G	GRCh38
NC_000002.11:g.10588038A>G , CM000664.1:g.10588038A>G	GRCh37
NC_000002.10:g.10505489A>G	NCBI36
NG_012105.1:g.5416T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000443218.2:c.-412T>C	ENSP00000390691.2:n.-412T>C
ENST00000446285.6:c.-128+209T>C	ENSP00000514632.1:n.-128+209T>C
ENST00000699835.1:c.-856T>C	ENSP00000514633.1:n.-856T>C
ENST00000699836.1:c.-18+209T>C	ENSP00000514634.1:n.-18+209T>C
ENST00000234111.9:c.-128+209T>C MANE Select	ENSP00000234111.4:n.-128+209T>C
ENST00000234111.8:c.-128+209T>C	ENSP00000234111.4:n.-128+209T>C
ENST00000446285.5:n.189+209T>C
NM_001287188.1:c.-415+209T>C	NP_001274117.1:n.-415+209T>C
NM_002539.2:c.-128+209T>C	NP_002530.1:n.-128+209T>C
NM_002539.3:c.-128+209T>C MANE Select	NP_002530.1:n.-128+209T>C
NM_001287188.2:c.-415+209T>C	NP_001274117.1:n.-415+209T>C
NM_001287189.2:c.-566T>C	NP_001274118.1:n.-566T>C
NM_001287190.2:c.-412T>C	NP_001274119.1:n.-412T>C