Canonical Allele Identifier: CA6977679

Gene: HTR2A

Linked Data

• dbSNP Id: rs779991888
• ExAC: 13:47469796 G / C
• gnomAD v2: 13-47469796-G-C
• gnomAD v3: 13-46895661-G-C
• gnomAD v4: 13-46895661-G-C
• MyVariant Identifiers: chr13:g.47469796G>C (hg19) ; chr13:g.46895661G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46895661G>C , CM000675.2:g.46895661G>C	GRCh38
NC_000013.10:g.47469796G>C , CM000675.1:g.47469796G>C	GRCh37
NC_000013.9:g.46367797G>C	NCBI36
NG_013011.1:g.6374C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.246C>G MANE Select	ENSP00000437737.1:p.Ala82=
ENST00000543956.5:c.-78+1013C>G	ENSP00000441861.2:n.-78+1013C>G
ENST00000378688.8:c.246C>G	ENSP00000367959.3:p.Ala82=
ENST00000542664.3:c.246C>G	ENSP00000437737.1:p.Ala82=
ENST00000543956.4:c.160+1013C>G	ENSP00000441861.1:n.160+1013C>G
ENST00000612998.1:c.153C>G	ENSP00000482708.1:p.Ala51=
NM_000621.4:c.246C>G	NP_000612.1:p.Ala82=
NM_001165947.2:c.160+1013C>G	NP_001159419.1:n.160+1013C>G
NM_000621.5:c.246C>G MANE Select	NP_000612.1:p.Ala82=
NM_001165947.5:c.-78+1013C>G	NP_001159419.2:n.-78+1013C>G
NM_001378924.1:c.246C>G	NP_001365853.1:p.Ala82=