Canonical Allele Identifier: CA388153060

Gene: HTR2A

Linked Data

• MyVariant Identifiers: chr13:g.47466657C>A (hg19) ; chr13:g.46892522C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46892522C>A , CM000675.2:g.46892522C>A	GRCh38
NC_000013.10:g.47466657C>A , CM000675.1:g.47466657C>A	GRCh37
NC_000013.9:g.46364658C>A	NCBI36
NG_013011.1:g.9513G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.481G>T MANE Select	ENSP00000437737.1:p.Ala161Ser
ENST00000543956.5:c.-9G>T	ENSP00000441861.2:n.-9G>T
ENST00000378688.8:c.481G>T	ENSP00000367959.3:p.Ala161Ser
ENST00000542664.3:c.481G>T	ENSP00000437737.1:p.Ala161Ser
ENST00000543956.4:c.229G>T	ENSP00000441861.1:p.Ala77Ser
NM_000621.4:c.481G>T	NP_000612.1:p.Ala161Ser
NM_001165947.2:c.229G>T	NP_001159419.1:p.Ala77Ser
NM_000621.5:c.481G>T MANE Select	NP_000612.1:p.Ala161Ser
NM_001165947.5:c.-9G>T	NP_001159419.2:n.-9G>T
NM_001378924.1:c.481G>T	NP_001365853.1:p.Ala161Ser