Canonical Allele Identifier: CA955689720

Gene: HTR2A

Linked Data

• gnomAD v3: 13-46845606-T-A
• gnomAD v4: 13-46845606-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46845606T>A , CM000675.2:g.46845606T>A	GRCh38
NC_000013.10:g.47419741T>A , CM000675.1:g.47419741T>A	GRCh37
NC_000013.9:g.46317742T>A	NCBI36
NG_013011.1:g.56429A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.614-9967A>T MANE Select	ENSP00000437737.1:n.614-9967A>T
ENST00000543956.5:c.125-9967A>T	ENSP00000441861.2:n.125-9967A>T
ENST00000378688.8:c.614-9967A>T	ENSP00000367959.3:n.614-9967A>T
ENST00000542664.3:c.614-9967A>T	ENSP00000437737.1:n.614-9967A>T
ENST00000543956.4:c.362-9967A>T	ENSP00000441861.1:n.362-9967A>T
NM_000621.4:c.614-9967A>T	NP_000612.1:n.614-9967A>T
NM_001165947.2:c.362-9967A>T	NP_001159419.1:n.362-9967A>T
NM_000621.5:c.614-9967A>T MANE Select	NP_000612.1:n.614-9967A>T
NM_001165947.5:c.125-9967A>T	NP_001159419.2:n.125-9967A>T
NM_001378924.1:c.614-9967A>T	NP_001365853.1:n.614-9967A>T