Canonical Allele Identifier: CA2622959681

Gene: HTR2A

Linked Data

• gnomAD v4: 13-46896017-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46896017C>A , CM000675.2:g.46896017C>A	GRCh38
NC_000013.10:g.47470152C>A , CM000675.1:g.47470152C>A	GRCh37
NC_000013.9:g.46368153C>A	NCBI36
NG_013011.1:g.6018G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.-111G>T MANE Select	ENSP00000437737.1:n.-111G>T
ENST00000543956.5:c.-78+657G>T	ENSP00000441861.2:n.-78+657G>T
ENST00000378688.8:c.-111G>T	ENSP00000367959.3:n.-111G>T
ENST00000542664.3:c.-111G>T	ENSP00000437737.1:n.-111G>T
ENST00000543956.4:c.160+657G>T	ENSP00000441861.1:n.160+657G>T
NM_000621.4:c.-111G>T	NP_000612.1:n.-111G>T
NM_001165947.2:c.160+657G>T	NP_001159419.1:n.160+657G>T
NM_000621.5:c.-111G>T MANE Select	NP_000612.1:n.-111G>T
NM_001165947.5:c.-78+657G>T	NP_001159419.2:n.-78+657G>T
NM_001378924.1:c.-111G>T	NP_001365853.1:n.-111G>T