Canonical Allele Identifier: CA388150120

Gene: HTR2A

Linked Data

• dbSNP Id: rs889852055
• MyVariant Identifiers: chr13:g.47408986C>G (hg19) ; chr13:g.46834851C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46834851C>G , CM000675.2:g.46834851C>G	GRCh38
NC_000013.10:g.47408986C>G , CM000675.1:g.47408986C>G	GRCh37
NC_000013.9:g.46306987C>G	NCBI36
NG_013011.1:g.67184G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.1402G>C MANE Select	ENSP00000437737.1:p.Val468Leu
ENST00000543956.5:c.913G>C	ENSP00000441861.2:p.Val305Leu
ENST00000378688.8:c.1402G>C	ENSP00000367959.3:p.Val468Leu
ENST00000542664.3:c.1402G>C	ENSP00000437737.1:p.Val468Leu
ENST00000543956.4:c.1150G>C	ENSP00000441861.1:p.Val384Leu
NM_000621.4:c.1402G>C	NP_000612.1:p.Val468Leu
NM_001165947.2:c.1150G>C	NP_001159419.1:p.Val384Leu
NM_000621.5:c.1402G>C MANE Select	NP_000612.1:p.Val468Leu
NM_001165947.5:c.913G>C	NP_001159419.2:p.Val305Leu
NM_001378924.1:c.1402G>C	NP_001365853.1:p.Val468Leu