Canonical Allele Identifier: CA513362160

Gene: COMT MIR4761

Linked Data

• MyVariant Identifiers: chr22:g.19951286T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19963763T>G , CM000684.2:g.19963763T>G	GRCh38
NC_000022.10:g.19951286T>G , CM000684.1:g.19951286T>G	GRCh37
NC_000022.9:g.18331286T>G	NCBI36
NG_011526.1:g.27024T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361682.11:c.483+4T>G (COMT) MANE Select	ENSP00000354511.6:n.483+4T>G
ENST00000428707.2:c.483+4T>G (COMT)	ENSP00000387695.2:n.483+4T>G
ENST00000676678.1:c.483+4T>G (COMT)	ENSP00000503719.1:n.483+4T>G
ENST00000677397.1:c.333+4T>G (COMT)	ENSP00000503422.1:n.333+4T>G
ENST00000677564.1:n.266+4T>G (COMT)
ENST00000677675.1:n.283+4T>G (COMT)
ENST00000678240.1:n.331+4T>G (COMT)
ENST00000678255.1:c.483+4T>G (COMT)	ENSP00000504402.1:n.483+4T>G
ENST00000678769.1:c.483+4T>G (COMT)	ENSP00000503289.1:n.483+4T>G
ENST00000678868.1:c.483+4T>G (COMT)	ENSP00000503583.1:n.483+4T>G
ENST00000678945.1:n.293+4T>G (COMT)
ENST00000207636.9:c.483+4T>G (COMT)	ENSP00000207636.5:n.483+4T>G
ENST00000361682.10:c.483+4T>G (COMT)	ENSP00000354511.6:n.483+4T>G
ENST00000403184.5:c.483+4T>G (COMT)	ENSP00000383966.1:n.483+4T>G
ENST00000403710.5:c.483+4T>G (COMT)	ENSP00000385917.1:n.483+4T>G
ENST00000406520.7:c.483+4T>G (COMT)	ENSP00000385150.3:n.483+4T>G
ENST00000407537.5:c.483+4T>G (COMT)	ENSP00000384654.2:n.483+4T>G
ENST00000412786.5:c.483+4T>G (COMT)	ENSP00000403958.1:n.483+4T>G
ENST00000428707.1:c.61+4T>G (COMT)
ENST00000449653.5:c.333+4T>G (COMT)	ENSP00000416778.1:n.333+4T>G
ENST00000493893.1:n.221+4T>G (COMT)
NM_000754.3:c.483+4T>G (COMT)	NP_000745.1:n.483+4T>G
NM_001135161.1:c.483+4T>G (COMT)	NP_001128633.1:n.483+4T>G
NM_001135162.1:c.483+4T>G (COMT)	NP_001128634.1:n.483+4T>G
NM_007310.2:c.333+4T>G (COMT)	NP_009294.1:n.333+4T>G
NR_039918.1:n.11T>G (MIR4761)
XM_011529885.1:c.597+4T>G (COMT)	XP_011528187.1:n.597+4T>G
XM_011529886.1:c.597+4T>G (COMT)	XP_011528188.1:n.597+4T>G
XM_011529887.1:c.483+4T>G (COMT)	XP_011528189.1:n.483+4T>G
XM_011529888.1:c.483+4T>G (COMT)	XP_011528190.1:n.483+4T>G
XM_011529889.1:c.483+4T>G (COMT)	XP_011528191.1:n.483+4T>G
XM_011529890.1:c.483+4T>G (COMT)	XP_011528192.1:n.483+4T>G
XM_011529891.1:c.483+4T>G (COMT)	XP_011528193.1:n.483+4T>G
NM_001362828.1:c.483+4T>G (COMT)	NP_001349757.1:n.483+4T>G
XM_011529886.2:c.894+4T>G (COMT)	XP_011528188.2:n.894+4T>G
XM_017028595.1:c.483+4T>G (COMT)	XP_016884084.1:n.483+4T>G
NM_000754.4:c.483+4T>G (COMT) MANE Select	NP_000745.1:n.483+4T>G
NM_001135161.2:c.483+4T>G (COMT)	NP_001128633.1:n.483+4T>G
NM_001135162.2:c.483+4T>G (COMT)	NP_001128634.1:n.483+4T>G
NM_001362828.2:c.483+4T>G (COMT)	NP_001349757.1:n.483+4T>G
NM_007310.3:c.333+4T>G (COMT)	NP_009294.1:n.333+4T>G