Canonical Allele Identifier: CA698546203

Gene: HTR2A

Linked Data

• dbSNP Id: rs1401462552
• gnomAD v3: 13-46895943-G-A
• gnomAD v4: 13-46895943-G-A
• MyVariant Identifiers: chr13:g.47470078G>A (hg19) ; chr13:g.46895943G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46895943G>A , CM000675.2:g.46895943G>A	GRCh38
NC_000013.10:g.47470078G>A , CM000675.1:g.47470078G>A	GRCh37
NC_000013.9:g.46368079G>A	NCBI36
NG_013011.1:g.6092C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.-37C>T MANE Select	ENSP00000437737.1:n.-37C>T
ENST00000543956.5:c.-78+731C>T	ENSP00000441861.2:n.-78+731C>T
ENST00000378688.8:c.-37C>T	ENSP00000367959.3:n.-37C>T
ENST00000542664.3:c.-37C>T	ENSP00000437737.1:n.-37C>T
ENST00000543956.4:c.160+731C>T	ENSP00000441861.1:n.160+731C>T
NM_000621.4:c.-37C>T	NP_000612.1:n.-37C>T
NM_001165947.2:c.160+731C>T	NP_001159419.1:n.160+731C>T
NM_000621.5:c.-37C>T MANE Select	NP_000612.1:n.-37C>T
NM_001165947.5:c.-78+731C>T	NP_001159419.2:n.-78+731C>T
NM_001378924.1:c.-37C>T	NP_001365853.1:n.-37C>T