Canonical Allele Identifier: CA2396115629

Gene: COMT

Linked Data

• dbSNP Id: rs1941755532

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19942533A>G , CM000684.2:g.19942533A>G	GRCh38
NC_000022.10:g.19930056A>G , CM000684.1:g.19930056A>G	GRCh37
NC_000022.9:g.18310056A>G	NCBI36
NG_011526.1:g.5794A>G
NG_011835.1:g.4304T>C , LRG_417:g.4304T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000361682.11:c.-92+636A>G MANE Select	ENSP00000354511.6:n.-92+636A>G
ENST00000428707.2:c.-92+636A>G	ENSP00000387695.2:n.-92+636A>G
ENST00000676678.1:c.-92+958A>G	ENSP00000503719.1:n.-92+958A>G
ENST00000678769.1:c.-92+636A>G	ENSP00000503289.1:n.-92+636A>G
ENST00000678868.1:c.-276+636A>G	ENSP00000503583.1:n.-276+636A>G
ENST00000361682.10:c.-92+636A>G	ENSP00000354511.6:n.-92+636A>G
ENST00000403184.5:c.-92+636A>G	ENSP00000383966.1:n.-92+636A>G
ENST00000403710.5:c.-386+636A>G	ENSP00000385917.1:n.-386+636A>G
ENST00000407537.5:c.-270+636A>G	ENSP00000384654.2:n.-270+636A>G
ENST00000467943.5:n.105+636A>G
NM_000754.3:c.-92+636A>G	NP_000745.1:n.-92+636A>G
XM_011529887.1:c.-92+636A>G	XP_011528189.1:n.-92+636A>G
XM_011529890.1:c.-386+636A>G	XP_011528192.1:n.-386+636A>G
XM_011529891.1:c.-386+358A>G	XP_011528193.1:n.-386+358A>G
NM_001362828.1:c.-386+636A>G	NP_001349757.1:n.-386+636A>G
XM_017028595.1:c.-386+358A>G	XP_016884084.1:n.-386+358A>G
NM_000754.4:c.-92+636A>G MANE Select	NP_000745.1:n.-92+636A>G
NM_001362828.2:c.-386+636A>G	NP_001349757.1:n.-386+636A>G