Canonical Allele Identifier: CA249263330

Gene: HTR2A

Linked Data

• dbSNP Id: rs925713749
• gnomAD v3: 13-46897062-C-T
• gnomAD v4: 13-46897062-C-T
• MyVariant Identifiers: chr13:g.47471197C>T (hg19) ; chr13:g.46897062C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46897062C>T , CM000675.2:g.46897062C>T	GRCh38
NC_000013.10:g.47471197C>T , CM000675.1:g.47471197C>T	GRCh37
NC_000013.9:g.46369198C>T	NCBI36
NG_013011.1:g.4973G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000543956.5:c.-466G>A	ENSP00000441861.2:n.-466G>A
ENST00000542664.3:c.-717G>A	ENSP00000437737.1:n.-717G>A
ENST00000543956.4:c.-229G>A	ENSP00000441861.1:n.-229G>A
NM_000621.4:c.-717G>A	NP_000612.1:n.-717G>A
NM_001165947.2:c.-229G>A	NP_001159419.1:n.-229G>A
NM_001378924.1:c.-328-828G>A	NP_001365853.1:n.-328-828G>A