Canonical Allele Identifier: CA698547202

Gene: HTR2A

Linked Data

• dbSNP Id: rs1336555216
• gnomAD v3: 13-46897315-A-G
• gnomAD v4: 13-46897315-A-G
• MyVariant Identifiers: chr13:g.47471450A>G (hg19) ; chr13:g.46897315A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46897315A>G , CM000675.2:g.46897315A>G	GRCh38
NC_000013.10:g.47471450A>G , CM000675.1:g.47471450A>G	GRCh37
NC_000013.9:g.46369451A>G	NCBI36
NG_013011.1:g.4720T>C

Transcript Alleles

HGVS	Amino-acid change
NM_001378924.1:c.-329+637T>C	NP_001365853.1:n.-329+637T>C