Canonical Allele Identifier: CA15790524
Gene: HTR2A HGNC NCBI
HTR2A-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs643627

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46854476T>C , CM000675.2:g.46854476T>C GRCh38
NC_000013.10:g.47428611T>C , CM000675.1:g.47428611T>C GRCh37
NC_000013.9:g.46326612T>C NCBI36
NG_013011.1:g.47559A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000542664.4:c.614-18837A>G MANE Select ENSP00000437737.1:p.=
ENST00000543956.5:c.125-18837A>G ENSP00000441861.2:p.=
ENST00000378688.8:c.614-18837A>G ENSP00000367959.3:p.=
ENST00000542664.3:c.614-18837A>G ENSP00000437737.1:p.=
ENST00000543956.4:c.362-18837A>G ENSP00000441861.1:p.=
NM_000621.4:c.614-18837A>G (HTR2A) NP_000612.1:p.=
NM_001165947.2:c.362-18837A>G (HTR2A) NP_001159419.1:p.=
NR_046612.1:n.231+394T>C (HTR2A-AS1)
NR_103752.1:n.88-1614T>C (HTR2A-AS1)
NM_000621.5:c.614-18837A>G (HTR2A) MANE Select NP_000612.1:p.=
NM_001165947.5:c.125-18837A>G (HTR2A) NP_001159419.2:p.=
NM_001378924.1:c.614-18837A>G (HTR2A) NP_001365853.1:p.=