Canonical Allele Identifier: CA483555018

Gene: HTR2A

Linked Data

• MyVariant Identifiers: chr13:g.47466658C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46892523C>G , CM000675.2:g.46892523C>G	GRCh38
NC_000013.10:g.47466658C>G , CM000675.1:g.47466658C>G	GRCh37
NC_000013.9:g.46364659C>G	NCBI36
NG_013011.1:g.9512G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.480G>C MANE Select	ENSP00000437737.1:p.Thr160=
ENST00000543956.5:c.-10G>C	ENSP00000441861.2:n.-10G>C
ENST00000378688.8:c.480G>C	ENSP00000367959.3:p.Thr160=
ENST00000542664.3:c.480G>C	ENSP00000437737.1:p.Thr160=
ENST00000543956.4:c.228G>C	ENSP00000441861.1:p.Thr76=
NM_000621.4:c.480G>C	NP_000612.1:p.Thr160=
NM_001165947.2:c.228G>C	NP_001159419.1:p.Thr76=
NM_000621.5:c.480G>C MANE Select	NP_000612.1:p.Thr160=
NM_001165947.5:c.-10G>C	NP_001159419.2:n.-10G>C
NM_001378924.1:c.480G>C	NP_001365853.1:p.Thr160=