Canonical Allele Identifier: CA2622958651

Gene: HTR2A

Linked Data

• gnomAD v4: 13-46834733-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46834733T>G , CM000675.2:g.46834733T>G	GRCh38
NC_000013.10:g.47408868T>G , CM000675.1:g.47408868T>G	GRCh37
NC_000013.9:g.46306869T>G	NCBI36
NG_013011.1:g.67302A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000542664.4:c.*104A>C MANE Select	ENSP00000437737.1:n.*104A>C
ENST00000543956.5:c.*104A>C	ENSP00000441861.2:n.*104A>C
ENST00000378688.8:c.*104A>C	ENSP00000367959.3:n.*104A>C
ENST00000542664.3:c.*104A>C	ENSP00000437737.1:n.*104A>C
ENST00000543956.4:c.*104A>C	ENSP00000441861.1:n.*104A>C
NM_000621.4:c.*104A>C	NP_000612.1:n.*104A>C
NM_001165947.2:c.*104A>C	NP_001159419.1:n.*104A>C
NM_000621.5:c.*104A>C MANE Select	NP_000612.1:n.*104A>C
NM_001165947.5:c.*104A>C	NP_001159419.2:n.*104A>C
NM_001378924.1:c.*104A>C	NP_001365853.1:n.*104A>C