Canonical Allele Identifier: CA698547103

Gene: HTR2A

Linked Data

• dbSNP Id: rs1261076150
• gnomAD v3: 13-46897153-C-A
• gnomAD v4: 13-46897153-C-A
• MyVariant Identifiers: chr13:g.47471288C>A (hg19) ; chr13:g.46897153C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46897153C>A , CM000675.2:g.46897153C>A	GRCh38
NC_000013.10:g.47471288C>A , CM000675.1:g.47471288C>A	GRCh37
NC_000013.9:g.46369289C>A	NCBI36
NG_013011.1:g.4882G>T

Transcript Alleles

HGVS	Amino-acid change
NM_001378924.1:c.-329+799G>T	NP_001365853.1:n.-329+799G>T