Canonical Allele Identifier: CA42456710

Gene: ODC1

Linked Data

• dbSNP Id: rs566793109
• gnomAD v2: 2-10587798-C-G
• gnomAD v3: 2-10447672-C-G
• gnomAD v4: 2-10447672-C-G
• MyVariant Identifiers: chr2:g.10587798C>G (hg19) ; chr2:g.10447672C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.10447672C>G , CM000664.2:g.10447672C>G	GRCh38
NC_000002.11:g.10587798C>G , CM000664.1:g.10587798C>G	GRCh37
NC_000002.10:g.10505249C>G	NCBI36
NG_012105.1:g.5656G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000443218.2:c.-172G>C	ENSP00000390691.2:n.-172G>C
ENST00000446285.6:c.-128+449G>C	ENSP00000514632.1:n.-128+449G>C
ENST00000699835.1:c.-616G>C	ENSP00000514633.1:n.-616G>C
ENST00000699836.1:c.-18+449G>C	ENSP00000514634.1:n.-18+449G>C
ENST00000234111.9:c.-128+449G>C MANE Select	ENSP00000234111.4:n.-128+449G>C
ENST00000234111.8:c.-128+449G>C	ENSP00000234111.4:n.-128+449G>C
ENST00000405333.5:c.-326G>C	ENSP00000385333.1:n.-326G>C
ENST00000443218.1:c.-172G>C	ENSP00000390691.1:n.-172G>C
ENST00000446285.5:n.189+449G>C
NM_001287188.1:c.-415+449G>C	NP_001274117.1:n.-415+449G>C
NM_001287189.1:c.-326G>C	NP_001274118.1:n.-326G>C
NM_001287190.1:c.-172G>C	NP_001274119.1:n.-172G>C
NM_002539.2:c.-128+449G>C	NP_002530.1:n.-128+449G>C
NM_002539.3:c.-128+449G>C MANE Select	NP_002530.1:n.-128+449G>C
NM_001287188.2:c.-415+449G>C	NP_001274117.1:n.-415+449G>C
NM_001287189.2:c.-326G>C	NP_001274118.1:n.-326G>C
NM_001287190.2:c.-172G>C	NP_001274119.1:n.-172G>C