Canonical Allele Identifier: CA609569561

Gene: HTR2A

Linked Data

• dbSNP Id: rs1361530433
• gnomAD v2: 13-47471471-G-C
• gnomAD v3: 13-46897336-G-C
• gnomAD v4: 13-46897336-G-C
• MyVariant Identifiers: chr13:g.47471471G>C (hg19) ; chr13:g.46897336G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46897336G>C , CM000675.2:g.46897336G>C	GRCh38
NC_000013.10:g.47471471G>C , CM000675.1:g.47471471G>C	GRCh37
NC_000013.9:g.46369472G>C	NCBI36
NG_013011.1:g.4699C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001378924.1:c.-329+616C>G	NP_001365853.1:n.-329+616C>G