Canonical Allele Identifier: CA6977487

Gene: HTR2A

Linked Data

• dbSNP Id: rs745333658
• ExAC: 13:47408984 C / T
• gnomAD v2: 13-47408984-C-T
• gnomAD v4: 13-46834849-C-T
• MyVariant Identifiers: chr13:g.47408984C>T (hg19) ; chr13:g.46834849C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46834849C>T , CM000675.2:g.46834849C>T	GRCh38
NC_000013.10:g.47408984C>T , CM000675.1:g.47408984C>T	GRCh37
NC_000013.9:g.46306985C>T	NCBI36
NG_013011.1:g.67186G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.1404G>A MANE Select	ENSP00000437737.1:p.Val468=
ENST00000543956.5:c.915G>A	ENSP00000441861.2:p.Val305=
ENST00000378688.8:c.1404G>A	ENSP00000367959.3:p.Val468=
ENST00000542664.3:c.1404G>A	ENSP00000437737.1:p.Val468=
ENST00000543956.4:c.1152G>A	ENSP00000441861.1:p.Val384=
NM_000621.4:c.1404G>A	NP_000612.1:p.Val468=
NM_001165947.2:c.1152G>A	NP_001159419.1:p.Val384=
NM_000621.5:c.1404G>A MANE Select	NP_000612.1:p.Val468=
NM_001165947.5:c.915G>A	NP_001159419.2:p.Val305=
NM_001378924.1:c.1404G>A	NP_001365853.1:p.Val468=