Canonical Allele Identifier: CA6977672

Gene: HTR2A

Linked Data

• dbSNP Id: rs758863570
• ExAC: 13:47469715 G / A
• gnomAD v2: 13-47469715-G-A
• gnomAD v3: 13-46895580-G-A
• gnomAD v4: 13-46895580-G-A
• MyVariant Identifiers: chr13:g.47469715G>A (hg19) ; chr13:g.46895580G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46895580G>A , CM000675.2:g.46895580G>A	GRCh38
NC_000013.10:g.47469715G>A , CM000675.1:g.47469715G>A	GRCh37
NC_000013.9:g.46367716G>A	NCBI36
NG_013011.1:g.6455C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.327C>T MANE Select	ENSP00000437737.1:p.Thr109=
ENST00000543956.5:c.-78+1094C>T	ENSP00000441861.2:n.-78+1094C>T
ENST00000378688.8:c.327C>T	ENSP00000367959.3:p.Thr109=
ENST00000542664.3:c.327C>T	ENSP00000437737.1:p.Thr109=
ENST00000543956.4:c.160+1094C>T	ENSP00000441861.1:n.160+1094C>T
ENST00000612998.1:c.234C>T	ENSP00000482708.1:p.Thr78=
NM_000621.4:c.327C>T	NP_000612.1:p.Thr109=
NM_001165947.2:c.160+1094C>T	NP_001159419.1:n.160+1094C>T
NM_000621.5:c.327C>T MANE Select	NP_000612.1:p.Thr109=
NM_001165947.5:c.-78+1094C>T	NP_001159419.2:n.-78+1094C>T
NM_001378924.1:c.327C>T	NP_001365853.1:p.Thr109=