Canonical Allele Identifier: CA388150996

Gene: HTR2A

Linked Data

• MyVariant Identifiers: chr13:g.47409193A>C (hg19) ; chr13:g.46835058A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46835058A>C , CM000675.2:g.46835058A>C	GRCh38
NC_000013.10:g.47409193A>C , CM000675.1:g.47409193A>C	GRCh37
NC_000013.9:g.46307194A>C	NCBI36
NG_013011.1:g.66977T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.1195T>G MANE Select	ENSP00000437737.1:p.Tyr399Asp
ENST00000543956.5:c.706T>G	ENSP00000441861.2:p.Tyr236Asp
ENST00000378688.8:c.1195T>G	ENSP00000367959.3:p.Tyr399Asp
ENST00000542664.3:c.1195T>G	ENSP00000437737.1:p.Tyr399Asp
ENST00000543956.4:c.943T>G	ENSP00000441861.1:p.Tyr315Asp
NM_000621.4:c.1195T>G	NP_000612.1:p.Tyr399Asp
NM_001165947.2:c.943T>G	NP_001159419.1:p.Tyr315Asp
NM_000621.5:c.1195T>G MANE Select	NP_000612.1:p.Tyr399Asp
NM_001165947.5:c.706T>G	NP_001159419.2:p.Tyr236Asp
NM_001378924.1:c.1195T>G	NP_001365853.1:p.Tyr399Asp