Canonical Allele Identifier: CA6977689

Gene: HTR2A

Linked Data

• dbSNP Id: rs763386955
• ExAC: 13:47469863 C / A
• gnomAD v2: 13-47469863-C-A
• gnomAD v4: 13-46895728-C-A
• MyVariant Identifiers: chr13:g.47469863C>A (hg19) ; chr13:g.46895728C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46895728C>A , CM000675.2:g.46895728C>A	GRCh38
NC_000013.10:g.47469863C>A , CM000675.1:g.47469863C>A	GRCh37
NC_000013.9:g.46367864C>A	NCBI36
NG_013011.1:g.6307G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.179G>T MANE Select	ENSP00000437737.1:p.Cys60Phe
ENST00000543956.5:c.-78+946G>T	ENSP00000441861.2:n.-78+946G>T
ENST00000378688.8:c.179G>T	ENSP00000367959.3:p.Cys60Phe
ENST00000542664.3:c.179G>T	ENSP00000437737.1:p.Cys60Phe
ENST00000543956.4:c.160+946G>T	ENSP00000441861.1:n.160+946G>T
ENST00000612998.1:c.86G>T	ENSP00000482708.1:p.Cys29Phe
NM_000621.4:c.179G>T	NP_000612.1:p.Cys60Phe
NM_001165947.2:c.160+946G>T	NP_001159419.1:n.160+946G>T
NM_000621.5:c.179G>T MANE Select	NP_000612.1:p.Cys60Phe
NM_001165947.5:c.-78+946G>T	NP_001159419.2:n.-78+946G>T
NM_001378924.1:c.179G>T	NP_001365853.1:p.Cys60Phe