Canonical Allele Identifier: CA13788091
Gene: HTR2A HGNC NCBI
HTR2A-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs2296972

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46854336A>C , CM000675.2:g.46854336A>C GRCh38
NC_000013.10:g.47428471A>C , CM000675.1:g.47428471A>C GRCh37
NC_000013.9:g.46326472A>C NCBI36
NG_013011.1:g.47699T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000542664.4:c.614-18697T>G (HTR2A) MANE Select ENSP00000437737.1:n.614-18697T>G
ENST00000543956.5:c.125-18697T>G (HTR2A) ENSP00000441861.2:n.125-18697T>G
ENST00000378688.8:c.614-18697T>G (HTR2A) ENSP00000367959.3:n.614-18697T>G
ENST00000542664.3:c.614-18697T>G (HTR2A) ENSP00000437737.1:n.614-18697T>G
ENST00000543956.4:c.362-18697T>G (HTR2A) ENSP00000441861.1:n.362-18697T>G
NM_000621.4:c.614-18697T>G (HTR2A) NP_000612.1:n.614-18697T>G
NM_001165947.2:c.362-18697T>G (HTR2A) NP_001159419.1:n.362-18697T>G
NR_046612.1:n.231+254A>C (HTR2A-AS1)
NR_103752.1:n.88-1754A>C (HTR2A-AS1)
NM_000621.5:c.614-18697T>G (HTR2A) MANE Select NP_000612.1:n.614-18697T>G
NM_001165947.5:c.125-18697T>G (HTR2A) NP_001159419.2:n.125-18697T>G
NM_001378924.1:c.614-18697T>G (HTR2A) NP_001365853.1:n.614-18697T>G