Canonical Allele Identifier: CA322111808
Gene: COMT HGNC NCBI

Linked Data

dbSNP Id: rs9306232

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19942491G>T , CM000684.2:g.19942491G>T GRCh38
NC_000022.10:g.19930014G>T , CM000684.1:g.19930014G>T GRCh37
NC_000022.9:g.18310014G>T NCBI36
NG_011526.1:g.5752G>T
NG_011835.1:g.4346C>A , LRG_417:g.4346C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000361682.11:c.-92+594G>T MANE Select ENSP00000354511.6:n.-92+594G>T
ENST00000428707.2:c.-92+594G>T ENSP00000387695.2:n.-92+594G>T
ENST00000676678.1:c.-92+916G>T ENSP00000503719.1:n.-92+916G>T
ENST00000678769.1:c.-92+594G>T ENSP00000503289.1:n.-92+594G>T
ENST00000678868.1:c.-276+594G>T ENSP00000503583.1:n.-276+594G>T
ENST00000361682.10:c.-92+594G>T ENSP00000354511.6:n.-92+594G>T
ENST00000403184.5:c.-92+594G>T ENSP00000383966.1:n.-92+594G>T
ENST00000403710.5:c.-386+594G>T ENSP00000385917.1:n.-386+594G>T
ENST00000407537.5:c.-270+594G>T ENSP00000384654.2:n.-270+594G>T
ENST00000467943.5:n.105+594G>T
NM_000754.3:c.-92+594G>T NP_000745.1:n.-92+594G>T
XM_011529887.1:c.-92+594G>T XP_011528189.1:n.-92+594G>T
XM_011529890.1:c.-386+594G>T XP_011528192.1:n.-386+594G>T
XM_011529891.1:c.-386+316G>T XP_011528193.1:n.-386+316G>T
NM_001362828.1:c.-386+594G>T NP_001349757.1:n.-386+594G>T
XM_017028595.1:c.-386+316G>T XP_016884084.1:n.-386+316G>T
NM_000754.4:c.-92+594G>T MANE Select NP_000745.1:n.-92+594G>T
NM_001362828.2:c.-386+594G>T NP_001349757.1:n.-386+594G>T