Canonical Allele Identifier: CA609564311

Gene: HTR2A

Linked Data

• dbSNP Id: rs922106776
• gnomAD v2: 13-47419847-G-A
• MyVariant Identifiers: chr13:g.47419847G>A (hg19) ; chr13:g.46845712G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46845712G>A , CM000675.2:g.46845712G>A	GRCh38
NC_000013.10:g.47419847G>A , CM000675.1:g.47419847G>A	GRCh37
NC_000013.9:g.46317848G>A	NCBI36
NG_013011.1:g.56323C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.614-10073C>T MANE Select	ENSP00000437737.1:n.614-10073C>T
ENST00000543956.5:c.125-10073C>T	ENSP00000441861.2:n.125-10073C>T
ENST00000378688.8:c.614-10073C>T	ENSP00000367959.3:n.614-10073C>T
ENST00000542664.3:c.614-10073C>T	ENSP00000437737.1:n.614-10073C>T
ENST00000543956.4:c.362-10073C>T	ENSP00000441861.1:n.362-10073C>T
NM_000621.4:c.614-10073C>T	NP_000612.1:n.614-10073C>T
NM_001165947.2:c.362-10073C>T	NP_001159419.1:n.362-10073C>T
NM_000621.5:c.614-10073C>T MANE Select	NP_000612.1:n.614-10073C>T
NM_001165947.5:c.125-10073C>T	NP_001159419.2:n.125-10073C>T
NM_001378924.1:c.614-10073C>T	NP_001365853.1:n.614-10073C>T