Canonical Allele Identifier: CA388152959

Gene: HTR2A

Linked Data

• MyVariant Identifiers: chr13:g.47466637G>T (hg19) ; chr13:g.46892502G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46892502G>T , CM000675.2:g.46892502G>T	GRCh38
NC_000013.10:g.47466637G>T , CM000675.1:g.47466637G>T	GRCh37
NC_000013.9:g.46364638G>T	NCBI36
NG_013011.1:g.9533C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.501C>A MANE Select	ENSP00000437737.1:p.Cys167Ter
ENST00000543956.5:c.12C>A	ENSP00000441861.2:p.Cys4Ter
ENST00000378688.8:c.501C>A	ENSP00000367959.3:p.Cys167Ter
ENST00000542664.3:c.501C>A	ENSP00000437737.1:p.Cys167Ter
ENST00000543956.4:c.249C>A	ENSP00000441861.1:p.Cys83Ter
NM_000621.4:c.501C>A	NP_000612.1:p.Cys167Ter
NM_001165947.2:c.249C>A	NP_001159419.1:p.Cys83Ter
NM_000621.5:c.501C>A MANE Select	NP_000612.1:p.Cys167Ter
NM_001165947.5:c.12C>A	NP_001159419.2:p.Cys4Ter
NM_001378924.1:c.501C>A	NP_001365853.1:p.Cys167Ter