Canonical Allele Identifier: CA15790972
Gene: HTR2A HGNC NCBI

Linked Data

dbSNP Id: rs2770296

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46866425C>T , CM000675.2:g.46866425C>T GRCh38
NC_000013.10:g.47440560C>T , CM000675.1:g.47440560C>T GRCh37
NC_000013.9:g.46338561C>T NCBI36
NG_013011.1:g.35610G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000542664.4:c.613+25965G>A MANE Select ENSP00000437737.1:p.=
ENST00000543956.5:c.124+25965G>A ENSP00000441861.2:p.=
ENST00000378688.8:c.613+25965G>A ENSP00000367959.3:p.=
ENST00000542664.3:c.613+25965G>A ENSP00000437737.1:p.=
ENST00000543956.4:c.361+25965G>A ENSP00000441861.1:p.=
NM_000621.4:c.613+25965G>A NP_000612.1:p.=
NM_001165947.2:c.361+25965G>A NP_001159419.1:p.=
NM_000621.5:c.613+25965G>A MANE Select NP_000612.1:p.=
NM_001165947.5:c.124+25965G>A NP_001159419.2:p.=
NM_001378924.1:c.613+25965G>A NP_001365853.1:p.=