Canonical Allele Identifier: CA14963959

Identifiers and link-outs to other resources

dbSNP Id: rs165599

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
NM_000754.3:c.*522G>A (COMT) VV NP_000745.1:p.=
NM_001135161.1:c.*522G>A (COMT) VV NP_001128633.1:p.=
NM_001135162.1:c.*522G>A (COMT) VV NP_001128634.1:p.=
NM_007310.2:c.*522G>A (COMT) VV NP_009294.1:p.=
XM_005261242.1:c.2764-2049C>T (ARVCF) XP_005261299.1:p.=
XM_006724243.1:c.2782-2049C>T (ARVCF) XP_006724306.1:p.=
XM_006724246.2:c.2536-2049C>T (ARVCF) XP_006724309.1:p.=
XM_011530179.1:c.2749-2049C>T (ARVCF) XP_011528481.1:p.=
XM_011530182.1:c.1348-2049C>T (ARVCF) XP_011528484.1:p.=
NM_001362828.1:c.*522G>A (COMT) VV NP_001349757.1:p.=
XM_005261242.3:c.2764-2049C>T (ARVCF) XP_005261299.1:p.=
XM_006724243.3:c.2782-2049C>T (ARVCF) XP_006724306.1:p.=
XM_006724246.4:c.2536-2049C>T (ARVCF) XP_006724309.1:p.=
XM_011530179.3:c.2749-2049C>T (ARVCF) XP_011528481.1:p.=
XM_011530182.3:c.1348-2049C>T (ARVCF) XP_011528484.1:p.=
XM_024452249.1:c.2536-2049C>T (ARVCF) XP_024308017.1:p.=
ENST00000361682.10:c.*522G>A ENSP00000354511.6:p.=