Canonical Allele Identifier: CA2396128793

Linked Data

dbSNP Id: rs165599

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19969258G>C , CM000684.2:g.19969258G>C GRCh38
NC_000022.10:g.19956781G>C , CM000684.1:g.19956781G>C GRCh37
NC_000022.9:g.18336781G>C NCBI36
NG_011526.1:g.32519G>C
NG_023326.1:g.52529C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000361682.11:c.*522G>C (COMT) MANE Select ENSP00000354511.6:n.*522G>C
ENST00000677564.1:n.1121G>C (COMT)
ENST00000678255.1:c.*522G>C (COMT) ENSP00000504402.1:n.*522G>C
ENST00000678769.1:c.*522G>C (COMT) ENSP00000503289.1:n.*522G>C
ENST00000678868.1:c.*522G>C (COMT) ENSP00000503583.1:n.*522G>C
ENST00000678945.1:n.1206G>C (COMT)
ENST00000361682.10:c.*522G>C (COMT) ENSP00000354511.6:n.*522G>C
NM_000754.3:c.*522G>C (COMT) NP_000745.1:n.*522G>C
NM_001135161.1:c.*522G>C (COMT) NP_001128633.1:n.*522G>C
NM_001135162.1:c.*522G>C (COMT) NP_001128634.1:n.*522G>C
NM_007310.2:c.*522G>C (COMT) NP_009294.1:n.*522G>C
XM_005261242.1:c.2764-2049C>G (ARVCF) XP_005261299.1:n.2764-2049C>G
XM_006724243.1:c.2782-2049C>G (ARVCF) XP_006724306.1:n.2782-2049C>G
XM_006724246.2:c.2536-2049C>G (ARVCF) XP_006724309.1:n.2536-2049C>G
XM_011530179.1:c.2749-2049C>G (ARVCF) XP_011528481.1:n.2749-2049C>G
XM_011530182.1:c.1348-2049C>G (ARVCF) XP_011528484.1:n.1348-2049C>G
NM_001362828.1:c.*522G>C (COMT) NP_001349757.1:n.*522G>C
XM_005261242.3:c.2764-2049C>G (ARVCF) XP_005261299.1:n.2764-2049C>G
XM_006724243.3:c.2782-2049C>G (ARVCF) XP_006724306.1:n.2782-2049C>G
XM_006724246.4:c.2536-2049C>G (ARVCF) XP_006724309.1:n.2536-2049C>G
XM_011530179.3:c.2749-2049C>G (ARVCF) XP_011528481.1:n.2749-2049C>G
XM_011530182.3:c.1348-2049C>G (ARVCF) XP_011528484.1:n.1348-2049C>G
XM_024452249.1:c.2536-2049C>G (ARVCF) XP_024308017.1:n.2536-2049C>G
NM_000754.4:c.*522G>C (COMT) MANE Select NP_000745.1:n.*522G>C
NM_001135161.2:c.*522G>C (COMT) NP_001128633.1:n.*522G>C
NM_001135162.2:c.*522G>C (COMT) NP_001128634.1:n.*522G>C
NM_001362828.2:c.*522G>C (COMT) NP_001349757.1:n.*522G>C
NM_007310.3:c.*522G>C (COMT) NP_009294.1:n.*522G>C