Canonical Allele Identifier: CA698547184

Gene: HTR2A

Linked Data

• dbSNP Id: rs1427824215
• gnomAD v3: 13-46897288-G-T
• gnomAD v4: 13-46897288-G-T
• MyVariant Identifiers: chr13:g.47471423G>T (hg19) ; chr13:g.46897288G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46897288G>T , CM000675.2:g.46897288G>T	GRCh38
NC_000013.10:g.47471423G>T , CM000675.1:g.47471423G>T	GRCh37
NC_000013.9:g.46369424G>T	NCBI36
NG_013011.1:g.4747C>A

Transcript Alleles

HGVS	Amino-acid change
NM_001378924.1:c.-329+664C>A	NP_001365853.1:n.-329+664C>A