Canonical Allele Identifier: CA388150677

Gene: HTR2A

Linked Data

• MyVariant Identifiers: chr13:g.47409135G>T (hg19) ; chr13:g.46835000G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46835000G>T , CM000675.2:g.46835000G>T	GRCh38
NC_000013.10:g.47409135G>T , CM000675.1:g.47409135G>T	GRCh37
NC_000013.9:g.46307136G>T	NCBI36
NG_013011.1:g.67035C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.1253C>A MANE Select	ENSP00000437737.1:p.Ala418Asp
ENST00000543956.5:c.764C>A	ENSP00000441861.2:p.Ala255Asp
ENST00000378688.8:c.1253C>A	ENSP00000367959.3:p.Ala418Asp
ENST00000542664.3:c.1253C>A	ENSP00000437737.1:p.Ala418Asp
ENST00000543956.4:c.1001C>A	ENSP00000441861.1:p.Ala334Asp
NM_000621.4:c.1253C>A	NP_000612.1:p.Ala418Asp
NM_001165947.2:c.1001C>A	NP_001159419.1:p.Ala334Asp
NM_000621.5:c.1253C>A MANE Select	NP_000612.1:p.Ala418Asp
NM_001165947.5:c.764C>A	NP_001159419.2:p.Ala255Asp
NM_001378924.1:c.1253C>A	NP_001365853.1:p.Ala418Asp