Canonical Allele Identifier: CA483555001

Gene: HTR2A

Linked Data

• dbSNP Id: rs746513298
• gnomAD v2: 13-47466628-C-A
• gnomAD v4: 13-46892493-C-A
• MyVariant Identifiers: chr13:g.47466628C>A (hg19) ; chr13:g.46892493C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46892493C>A , CM000675.2:g.46892493C>A	GRCh38
NC_000013.10:g.47466628C>A , CM000675.1:g.47466628C>A	GRCh37
NC_000013.9:g.46364629C>A	NCBI36
NG_013011.1:g.9542G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.510G>T MANE Select	ENSP00000437737.1:p.Ser170=
ENST00000543956.5:c.21G>T	ENSP00000441861.2:p.Ser7=
ENST00000378688.8:c.510G>T	ENSP00000367959.3:p.Ser170=
ENST00000542664.3:c.510G>T	ENSP00000437737.1:p.Ser170=
ENST00000543956.4:c.258G>T	ENSP00000441861.1:p.Ser86=
NM_000621.4:c.510G>T	NP_000612.1:p.Ser170=
NM_001165947.2:c.258G>T	NP_001159419.1:p.Ser86=
NM_000621.5:c.510G>T MANE Select	NP_000612.1:p.Ser170=
NM_001165947.5:c.21G>T	NP_001159419.2:p.Ser7=
NM_001378924.1:c.510G>T	NP_001365853.1:p.Ser170=