Canonical Allele Identifier: CA6977691

Gene: HTR2A

Linked Data

• dbSNP Id: rs566620377
• ExAC: 13:47469865 C / G
• gnomAD v2: 13-47469865-C-G
• gnomAD v4: 13-46895730-C-G
• MyVariant Identifiers: chr13:g.47469865C>G (hg19) ; chr13:g.46895730C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46895730C>G , CM000675.2:g.46895730C>G	GRCh38
NC_000013.10:g.47469865C>G , CM000675.1:g.47469865C>G	GRCh37
NC_000013.9:g.46367866C>G	NCBI36
NG_013011.1:g.6305G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.177G>C MANE Select	ENSP00000437737.1:p.Gly59=
ENST00000543956.5:c.-78+944G>C	ENSP00000441861.2:n.-78+944G>C
ENST00000378688.8:c.177G>C	ENSP00000367959.3:p.Gly59=
ENST00000542664.3:c.177G>C	ENSP00000437737.1:p.Gly59=
ENST00000543956.4:c.160+944G>C	ENSP00000441861.1:n.160+944G>C
ENST00000612998.1:c.84G>C	ENSP00000482708.1:p.Gly28=
NM_000621.4:c.177G>C	NP_000612.1:p.Gly59=
NM_001165947.2:c.160+944G>C	NP_001159419.1:n.160+944G>C
NM_000621.5:c.177G>C MANE Select	NP_000612.1:p.Gly59=
NM_001165947.5:c.-78+944G>C	NP_001159419.2:n.-78+944G>C
NM_001378924.1:c.177G>C	NP_001365853.1:p.Gly59=