Canonical Allele Identifier: CA609569553

Gene: HTR2A

Linked Data

• dbSNP Id: rs1324072227
• gnomAD v2: 13-47471233-A-G
• gnomAD v3: 13-46897098-A-G
• gnomAD v4: 13-46897098-A-G
• MyVariant Identifiers: chr13:g.47471233A>G (hg19) ; chr13:g.46897098A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46897098A>G , CM000675.2:g.46897098A>G	GRCh38
NC_000013.10:g.47471233A>G , CM000675.1:g.47471233A>G	GRCh37
NC_000013.9:g.46369234A>G	NCBI36
NG_013011.1:g.4937T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001378924.1:c.-329+854T>C	NP_001365853.1:n.-329+854T>C