Canonical Allele Identifier: CA698546253

Gene: HTR2A

Linked Data

• dbSNP Id: rs1384854895
• MyVariant Identifiers: chr13:g.47470203T>A (hg19) ; chr13:g.46896068T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46896068T>A , CM000675.2:g.46896068T>A	GRCh38
NC_000013.10:g.47470203T>A , CM000675.1:g.47470203T>A	GRCh37
NC_000013.9:g.46368204T>A	NCBI36
NG_013011.1:g.5967A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.-162A>T MANE Select	ENSP00000437737.1:n.-162A>T
ENST00000543956.5:c.-78+606A>T	ENSP00000441861.2:n.-78+606A>T
ENST00000542664.3:c.-162A>T	ENSP00000437737.1:n.-162A>T
ENST00000543956.4:c.160+606A>T	ENSP00000441861.1:n.160+606A>T
NM_000621.4:c.-162A>T	NP_000612.1:n.-162A>T
NM_001165947.2:c.160+606A>T	NP_001159419.1:n.160+606A>T
NM_000621.5:c.-162A>T MANE Select	NP_000612.1:n.-162A>T
NM_001165947.5:c.-78+606A>T	NP_001159419.2:n.-78+606A>T
NM_001378924.1:c.-162A>T	NP_001365853.1:n.-162A>T