Canonical Allele Identifier: CA483555238

Gene: HTR2A

Linked Data

• MyVariant Identifiers: chr13:g.47469763T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46895628T>A , CM000675.2:g.46895628T>A	GRCh38
NC_000013.10:g.47469763T>A , CM000675.1:g.47469763T>A	GRCh37
NC_000013.9:g.46367764T>A	NCBI36
NG_013011.1:g.6407A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000542664.4:c.279A>T MANE Select	ENSP00000437737.1:p.Ile93=
ENST00000543956.5:c.-78+1046A>T	ENSP00000441861.2:n.-78+1046A>T
ENST00000378688.8:c.279A>T	ENSP00000367959.3:p.Ile93=
ENST00000542664.3:c.279A>T	ENSP00000437737.1:p.Ile93=
ENST00000543956.4:c.160+1046A>T	ENSP00000441861.1:n.160+1046A>T
ENST00000612998.1:c.186A>T	ENSP00000482708.1:p.Ile62=
NM_000621.4:c.279A>T	NP_000612.1:p.Ile93=
NM_001165947.2:c.160+1046A>T	NP_001159419.1:n.160+1046A>T
NM_000621.5:c.279A>T MANE Select	NP_000612.1:p.Ile93=
NM_001165947.5:c.-78+1046A>T	NP_001159419.2:n.-78+1046A>T
NM_001378924.1:c.279A>T	NP_001365853.1:p.Ile93=