Canonical Allele Identifier: CA388153380

Gene: HTR2A

Linked Data

• MyVariant Identifiers: chr13:g.47466725C>A (hg19) ; chr13:g.46892590C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46892590C>A , CM000675.2:g.46892590C>A	GRCh38
NC_000013.10:g.47466725C>A , CM000675.1:g.47466725C>A	GRCh37
NC_000013.9:g.46364726C>A	NCBI36
NG_013011.1:g.9445G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.413G>T MANE Select	ENSP00000437737.1:p.Gly138Val
ENST00000543956.5:c.-77G>T	ENSP00000441861.2:n.-77G>T
ENST00000378688.8:c.413G>T	ENSP00000367959.3:p.Gly138Val
ENST00000542664.3:c.413G>T	ENSP00000437737.1:p.Gly138Val
ENST00000543956.4:c.161G>T	ENSP00000441861.1:p.Trp54Leu
NM_000621.4:c.413G>T	NP_000612.1:p.Gly138Val
NM_001165947.2:c.161G>T	NP_001159419.1:p.Trp54Leu
NM_000621.5:c.413G>T MANE Select	NP_000612.1:p.Gly138Val
NM_001165947.5:c.-77G>T	NP_001159419.2:n.-77G>T
NM_001378924.1:c.413G>T	NP_001365853.1:p.Gly138Val