Canonical Allele Identifier: CA322111832

Gene: COMT

Linked Data

• dbSNP Id: rs566115500
• gnomAD v3: 22-19942596-G-C
• gnomAD v4: 22-19942596-G-C
• MyVariant Identifiers: chr22:g.19930119G>C (hg19) ; chr22:g.19942596G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19942596G>C , CM000684.2:g.19942596G>C	GRCh38
NC_000022.10:g.19930119G>C , CM000684.1:g.19930119G>C	GRCh37
NC_000022.9:g.18310119G>C	NCBI36
NG_011526.1:g.5857G>C
NG_011835.1:g.4241C>G , LRG_417:g.4241C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000361682.11:c.-92+699G>C MANE Select	ENSP00000354511.6:n.-92+699G>C
ENST00000428707.2:c.-92+699G>C	ENSP00000387695.2:n.-92+699G>C
ENST00000676678.1:c.-92+1021G>C	ENSP00000503719.1:n.-92+1021G>C
ENST00000678769.1:c.-92+699G>C	ENSP00000503289.1:n.-92+699G>C
ENST00000678868.1:c.-276+699G>C	ENSP00000503583.1:n.-276+699G>C
ENST00000361682.10:c.-92+699G>C	ENSP00000354511.6:n.-92+699G>C
ENST00000403184.5:c.-92+699G>C	ENSP00000383966.1:n.-92+699G>C
ENST00000403710.5:c.-386+699G>C	ENSP00000385917.1:n.-386+699G>C
ENST00000407537.5:c.-270+699G>C	ENSP00000384654.2:n.-270+699G>C
ENST00000467943.5:n.105+699G>C
NM_000754.3:c.-92+699G>C	NP_000745.1:n.-92+699G>C
XM_011529887.1:c.-92+699G>C	XP_011528189.1:n.-92+699G>C
XM_011529890.1:c.-386+699G>C	XP_011528192.1:n.-386+699G>C
XM_011529891.1:c.-386+421G>C	XP_011528193.1:n.-386+421G>C
NM_001362828.1:c.-386+699G>C	NP_001349757.1:n.-386+699G>C
XM_017028595.1:c.-386+421G>C	XP_016884084.1:n.-386+421G>C
NM_000754.4:c.-92+699G>C MANE Select	NP_000745.1:n.-92+699G>C
NM_001362828.2:c.-386+699G>C	NP_001349757.1:n.-386+699G>C