Canonical Allele Identifier: CA388152969

Gene: HTR2A

Linked Data

• MyVariant Identifiers: chr13:g.47466639A>G (hg19) ; chr13:g.46892504A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46892504A>G , CM000675.2:g.46892504A>G	GRCh38
NC_000013.10:g.47466639A>G , CM000675.1:g.47466639A>G	GRCh37
NC_000013.9:g.46364640A>G	NCBI36
NG_013011.1:g.9531T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.499T>C MANE Select	ENSP00000437737.1:p.Cys167Arg
ENST00000543956.5:c.10T>C	ENSP00000441861.2:p.Cys4Arg
ENST00000378688.8:c.499T>C	ENSP00000367959.3:p.Cys167Arg
ENST00000542664.3:c.499T>C	ENSP00000437737.1:p.Cys167Arg
ENST00000543956.4:c.247T>C	ENSP00000441861.1:p.Cys83Arg
NM_000621.4:c.499T>C	NP_000612.1:p.Cys167Arg
NM_001165947.2:c.247T>C	NP_001159419.1:p.Cys83Arg
NM_000621.5:c.499T>C MANE Select	NP_000612.1:p.Cys167Arg
NM_001165947.5:c.10T>C	NP_001159419.2:p.Cys4Arg
NM_001378924.1:c.499T>C	NP_001365853.1:p.Cys167Arg