Canonical Allele Identifier: CA698547171

Gene: HTR2A

Linked Data

• dbSNP Id: rs1026918181
• gnomAD v3: 13-46897254-G-A
• gnomAD v4: 13-46897254-G-A
• MyVariant Identifiers: chr13:g.47471389G>A (hg19) ; chr13:g.46897254G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46897254G>A , CM000675.2:g.46897254G>A	GRCh38
NC_000013.10:g.47471389G>A , CM000675.1:g.47471389G>A	GRCh37
NC_000013.9:g.46369390G>A	NCBI36
NG_013011.1:g.4781C>T

Transcript Alleles

HGVS	Amino-acid change
NM_001378924.1:c.-329+698C>T	NP_001365853.1:n.-329+698C>T