Canonical Allele Identifier: CA388150929

Gene: HTR2A

Linked Data

• gnomAD v4: 13-46835048-T-C
• MyVariant Identifiers: chr13:g.47409183T>C (hg19) ; chr13:g.46835048T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46835048T>C , CM000675.2:g.46835048T>C	GRCh38
NC_000013.10:g.47409183T>C , CM000675.1:g.47409183T>C	GRCh37
NC_000013.9:g.46307184T>C	NCBI36
NG_013011.1:g.66987A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.1205A>G MANE Select	ENSP00000437737.1:p.Asn402Ser
ENST00000543956.5:c.716A>G	ENSP00000441861.2:p.Asn239Ser
ENST00000378688.8:c.1205A>G	ENSP00000367959.3:p.Asn402Ser
ENST00000542664.3:c.1205A>G	ENSP00000437737.1:p.Asn402Ser
ENST00000543956.4:c.953A>G	ENSP00000441861.1:p.Asn318Ser
NM_000621.4:c.1205A>G	NP_000612.1:p.Asn402Ser
NM_001165947.2:c.953A>G	NP_001159419.1:p.Asn318Ser
NM_000621.5:c.1205A>G MANE Select	NP_000612.1:p.Asn402Ser
NM_001165947.5:c.716A>G	NP_001159419.2:p.Asn239Ser
NM_001378924.1:c.1205A>G	NP_001365853.1:p.Asn402Ser