Canonical Allele Identifier: CA388150334

Gene: HTR2A

Linked Data

• gnomAD v4: 13-46834917-C-T
• MyVariant Identifiers: chr13:g.47409052C>T (hg19) ; chr13:g.46834917C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46834917C>T , CM000675.2:g.46834917C>T	GRCh38
NC_000013.10:g.47409052C>T , CM000675.1:g.47409052C>T	GRCh37
NC_000013.9:g.46307053C>T	NCBI36
NG_013011.1:g.67118G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.1336G>A MANE Select	ENSP00000437737.1:p.Val446Ile
ENST00000543956.5:c.847G>A	ENSP00000441861.2:p.Val283Ile
ENST00000378688.8:c.1336G>A	ENSP00000367959.3:p.Val446Ile
ENST00000542664.3:c.1336G>A	ENSP00000437737.1:p.Val446Ile
ENST00000543956.4:c.1084G>A	ENSP00000441861.1:p.Val362Ile
NM_000621.4:c.1336G>A	NP_000612.1:p.Val446Ile
NM_001165947.2:c.1084G>A	NP_001159419.1:p.Val362Ile
NM_000621.5:c.1336G>A MANE Select	NP_000612.1:p.Val446Ile
NM_001165947.5:c.847G>A	NP_001159419.2:p.Val283Ile
NM_001378924.1:c.1336G>A	NP_001365853.1:p.Val446Ile