Canonical Allele Identifier: CA388150924

Gene: HTR2A

Linked Data

• dbSNP Id: rs1423640595
• gnomAD v2: 13-47409182-G-T
• gnomAD v3: 13-46835047-G-T
• gnomAD v4: 13-46835047-G-T
• MyVariant Identifiers: chr13:g.47409182G>T (hg19) ; chr13:g.46835047G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46835047G>T , CM000675.2:g.46835047G>T	GRCh38
NC_000013.10:g.47409182G>T , CM000675.1:g.47409182G>T	GRCh37
NC_000013.9:g.46307183G>T	NCBI36
NG_013011.1:g.66988C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.1206C>A MANE Select	ENSP00000437737.1:p.Asn402Lys
ENST00000543956.5:c.717C>A	ENSP00000441861.2:p.Asn239Lys
ENST00000378688.8:c.1206C>A	ENSP00000367959.3:p.Asn402Lys
ENST00000542664.3:c.1206C>A	ENSP00000437737.1:p.Asn402Lys
ENST00000543956.4:c.954C>A	ENSP00000441861.1:p.Asn318Lys
NM_000621.4:c.1206C>A	NP_000612.1:p.Asn402Lys
NM_001165947.2:c.954C>A	NP_001159419.1:p.Asn318Lys
NM_000621.5:c.1206C>A MANE Select	NP_000612.1:p.Asn402Lys
NM_001165947.5:c.717C>A	NP_001159419.2:p.Asn239Lys
NM_001378924.1:c.1206C>A	NP_001365853.1:p.Asn402Lys