Canonical Allele Identifier: CA609569558

Gene: HTR2A

Linked Data

• dbSNP Id: rs1411501087
• gnomAD v2: 13-47471429-A-C
• gnomAD v3: 13-46897294-A-C
• gnomAD v4: 13-46897294-A-C
• MyVariant Identifiers: chr13:g.47471429A>C (hg19) ; chr13:g.46897294A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46897294A>C , CM000675.2:g.46897294A>C	GRCh38
NC_000013.10:g.47471429A>C , CM000675.1:g.47471429A>C	GRCh37
NC_000013.9:g.46369430A>C	NCBI36
NG_013011.1:g.4741T>G

Transcript Alleles

HGVS	Amino-acid change
NM_001378924.1:c.-329+658T>G	NP_001365853.1:n.-329+658T>G