Canonical Allele Identifier: CA388150353

Gene: HTR2A

Linked Data

• gnomAD v4: 13-46834920-T-C
• MyVariant Identifiers: chr13:g.47409055T>C (hg19) ; chr13:g.46834920T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46834920T>C , CM000675.2:g.46834920T>C	GRCh38
NC_000013.10:g.47409055T>C , CM000675.1:g.47409055T>C	GRCh37
NC_000013.9:g.46307056T>C	NCBI36
NG_013011.1:g.67115A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.1333A>G MANE Select	ENSP00000437737.1:p.Met445Val
ENST00000543956.5:c.844A>G	ENSP00000441861.2:p.Met282Val
ENST00000378688.8:c.1333A>G	ENSP00000367959.3:p.Met445Val
ENST00000542664.3:c.1333A>G	ENSP00000437737.1:p.Met445Val
ENST00000543956.4:c.1081A>G	ENSP00000441861.1:p.Met361Val
NM_000621.4:c.1333A>G	NP_000612.1:p.Met445Val
NM_001165947.2:c.1081A>G	NP_001159419.1:p.Met361Val
NM_000621.5:c.1333A>G MANE Select	NP_000612.1:p.Met445Val
NM_001165947.5:c.844A>G	NP_001159419.2:p.Met282Val
NM_001378924.1:c.1333A>G	NP_001365853.1:p.Met445Val