Canonical Allele Identifier: CA249262125

Gene: HTR2A

Linked Data

• dbSNP Id: rs1043732808
• gnomAD v2: 13-47469746-A-G
• MyVariant Identifiers: chr13:g.47469746A>G (hg19) ; chr13:g.46895611A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46895611A>G , CM000675.2:g.46895611A>G	GRCh38
NC_000013.10:g.47469746A>G , CM000675.1:g.47469746A>G	GRCh37
NC_000013.9:g.46367747A>G	NCBI36
NG_013011.1:g.6424T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.296T>C MANE Select	ENSP00000437737.1:p.Val99Ala
ENST00000543956.5:c.-78+1063T>C	ENSP00000441861.2:n.-78+1063T>C
ENST00000378688.8:c.296T>C	ENSP00000367959.3:p.Val99Ala
ENST00000542664.3:c.296T>C	ENSP00000437737.1:p.Val99Ala
ENST00000543956.4:c.160+1063T>C	ENSP00000441861.1:n.160+1063T>C
ENST00000612998.1:c.203T>C	ENSP00000482708.1:p.Val68Ala
NM_000621.4:c.296T>C	NP_000612.1:p.Val99Ala
NM_001165947.2:c.160+1063T>C	NP_001159419.1:n.160+1063T>C
NM_000621.5:c.296T>C MANE Select	NP_000612.1:p.Val99Ala
NM_001165947.5:c.-78+1063T>C	NP_001159419.2:n.-78+1063T>C
NM_001378924.1:c.296T>C	NP_001365853.1:p.Val99Ala