Canonical Allele Identifier: CA249246052

Gene: HTR2A

Linked Data

• dbSNP Id: rs930638262
• MyVariant Identifiers: chr13:g.47445870T>C (hg19) ; chr13:g.46871735T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46871735T>C , CM000675.2:g.46871735T>C	GRCh38
NC_000013.10:g.47445870T>C , CM000675.1:g.47445870T>C	GRCh37
NC_000013.9:g.46343871T>C	NCBI36
NG_013011.1:g.30300A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.613+20655A>G MANE Select	ENSP00000437737.1:n.613+20655A>G
ENST00000543956.5:c.124+20655A>G	ENSP00000441861.2:n.124+20655A>G
ENST00000378688.8:c.613+20655A>G	ENSP00000367959.3:n.613+20655A>G
ENST00000542664.3:c.613+20655A>G	ENSP00000437737.1:n.613+20655A>G
ENST00000543956.4:c.361+20655A>G	ENSP00000441861.1:n.361+20655A>G
NM_000621.4:c.613+20655A>G	NP_000612.1:n.613+20655A>G
NM_001165947.2:c.361+20655A>G	NP_001159419.1:n.361+20655A>G
NM_000621.5:c.613+20655A>G MANE Select	NP_000612.1:n.613+20655A>G
NM_001165947.5:c.124+20655A>G	NP_001159419.2:n.124+20655A>G
NM_001378924.1:c.613+20655A>G	NP_001365853.1:n.613+20655A>G