Canonical Allele Identifier: CA249252390

Gene: HTR2A

Linked Data

• dbSNP Id: rs927087168
• gnomAD v2: 13-47455147-A-G
• gnomAD v3: 13-46881012-A-G
• gnomAD v4: 13-46881012-A-G
• MyVariant Identifiers: chr13:g.47455147A>G (hg19) ; chr13:g.46881012A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46881012A>G , CM000675.2:g.46881012A>G	GRCh38
NC_000013.10:g.47455147A>G , CM000675.1:g.47455147A>G	GRCh37
NC_000013.9:g.46353148A>G	NCBI36
NG_013011.1:g.21023T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.613+11378T>C MANE Select	ENSP00000437737.1:n.613+11378T>C
ENST00000543956.5:c.124+11378T>C	ENSP00000441861.2:n.124+11378T>C
ENST00000378688.8:c.613+11378T>C	ENSP00000367959.3:n.613+11378T>C
ENST00000542664.3:c.613+11378T>C	ENSP00000437737.1:n.613+11378T>C
ENST00000543956.4:c.361+11378T>C	ENSP00000441861.1:n.361+11378T>C
NM_000621.4:c.613+11378T>C	NP_000612.1:n.613+11378T>C
NM_001165947.2:c.361+11378T>C	NP_001159419.1:n.361+11378T>C
NM_000621.5:c.613+11378T>C MANE Select	NP_000612.1:n.613+11378T>C
NM_001165947.5:c.124+11378T>C	NP_001159419.2:n.124+11378T>C
NM_001378924.1:c.613+11378T>C	NP_001365853.1:n.613+11378T>C