Canonical Allele Identifier: CA388150225

Gene: HTR2A

Linked Data

• dbSNP Id: rs1010455882
• MyVariant Identifiers: chr13:g.47409022C>G (hg19) ; chr13:g.46834887C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46834887C>G , CM000675.2:g.46834887C>G	GRCh38
NC_000013.10:g.47409022C>G , CM000675.1:g.47409022C>G	GRCh37
NC_000013.9:g.46307023C>G	NCBI36
NG_013011.1:g.67148G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.1366G>C MANE Select	ENSP00000437737.1:p.Ala456Pro
ENST00000543956.5:c.877G>C	ENSP00000441861.2:p.Ala293Pro
ENST00000378688.8:c.1366G>C	ENSP00000367959.3:p.Ala456Pro
ENST00000542664.3:c.1366G>C	ENSP00000437737.1:p.Ala456Pro
ENST00000543956.4:c.1114G>C	ENSP00000441861.1:p.Ala372Pro
NM_000621.4:c.1366G>C	NP_000612.1:p.Ala456Pro
NM_001165947.2:c.1114G>C	NP_001159419.1:p.Ala372Pro
NM_000621.5:c.1366G>C MANE Select	NP_000612.1:p.Ala456Pro
NM_001165947.5:c.877G>C	NP_001159419.2:p.Ala293Pro
NM_001378924.1:c.1366G>C	NP_001365853.1:p.Ala456Pro