Canonical Allele Identifier: CA388154734

Gene: HTR2A

Linked Data

• MyVariant Identifiers: chr13:g.47469887C>G (hg19) ; chr13:g.46895752C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46895752C>G , CM000675.2:g.46895752C>G	GRCh38
NC_000013.10:g.47469887C>G , CM000675.1:g.47469887C>G	GRCh37
NC_000013.9:g.46367888C>G	NCBI36
NG_013011.1:g.6283G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.155G>C MANE Select	ENSP00000437737.1:p.Arg52Pro
ENST00000543956.5:c.-78+922G>C	ENSP00000441861.2:n.-78+922G>C
ENST00000378688.8:c.155G>C	ENSP00000367959.3:p.Arg52Pro
ENST00000542664.3:c.155G>C	ENSP00000437737.1:p.Arg52Pro
ENST00000543956.4:c.160+922G>C	ENSP00000441861.1:n.160+922G>C
ENST00000612998.1:c.62G>C	ENSP00000482708.1:p.Arg21Pro
NM_000621.4:c.155G>C	NP_000612.1:p.Arg52Pro
NM_001165947.2:c.160+922G>C	NP_001159419.1:n.160+922G>C
NM_000621.5:c.155G>C MANE Select	NP_000612.1:p.Arg52Pro
NM_001165947.5:c.-78+922G>C	NP_001159419.2:n.-78+922G>C
NM_001378924.1:c.155G>C	NP_001365853.1:p.Arg52Pro