Canonical Allele Identifier: CA13788097
Gene: HTR2A HGNC NCBI

Linked Data

dbSNP Id: rs659734

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46861148G>A , CM000675.2:g.46861148G>A GRCh38
NC_000013.10:g.47435283G>A , CM000675.1:g.47435283G>A GRCh37
NC_000013.9:g.46333284G>A NCBI36
NG_013011.1:g.40887C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000542664.4:c.614-25509C>T MANE Select ENSP00000437737.1:p.=
ENST00000543956.5:c.125-25509C>T ENSP00000441861.2:p.=
ENST00000378688.8:c.614-25509C>T ENSP00000367959.3:p.=
ENST00000542664.3:c.614-25509C>T ENSP00000437737.1:p.=
ENST00000543956.4:c.362-25509C>T ENSP00000441861.1:p.=
NM_000621.4:c.614-25509C>T NP_000612.1:p.=
NM_001165947.2:c.362-25509C>T NP_001159419.1:p.=
NM_000621.5:c.614-25509C>T MANE Select NP_000612.1:p.=
NM_001165947.5:c.125-25509C>T NP_001159419.2:p.=
NM_001378924.1:c.614-25509C>T NP_001365853.1:p.=