Canonical Allele Identifier: CA6977638

Gene: HTR2A

Linked Data

• dbSNP Id: rs771701886
• ExAC: 13:47466621 G / A
• gnomAD v2: 13-47466621-G-A
• gnomAD v4: 13-46892486-G-A
• MyVariant Identifiers: chr13:g.47466621G>A (hg19) ; chr13:g.46892486G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46892486G>A , CM000675.2:g.46892486G>A	GRCh38
NC_000013.10:g.47466621G>A , CM000675.1:g.47466621G>A	GRCh37
NC_000013.9:g.46364622G>A	NCBI36
NG_013011.1:g.9549C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.517C>T MANE Select	ENSP00000437737.1:p.Arg173Cys
ENST00000543956.5:c.28C>T	ENSP00000441861.2:p.Arg10Cys
ENST00000378688.8:c.517C>T	ENSP00000367959.3:p.Arg173Cys
ENST00000542664.3:c.517C>T	ENSP00000437737.1:p.Arg173Cys
ENST00000543956.4:c.265C>T	ENSP00000441861.1:p.Arg89Cys
NM_000621.4:c.517C>T	NP_000612.1:p.Arg173Cys
NM_001165947.2:c.265C>T	NP_001159419.1:p.Arg89Cys
NM_000621.5:c.517C>T MANE Select	NP_000612.1:p.Arg173Cys
NM_001165947.5:c.28C>T	NP_001159419.2:p.Arg10Cys
NM_001378924.1:c.517C>T	NP_001365853.1:p.Arg173Cys