Canonical Allele Identifier: CA13811817
Gene: HTR2A HGNC NCBI

Linked Data

dbSNP Id: rs2070037

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46892935T>C , CM000675.2:g.46892935T>C GRCh38
NC_000013.10:g.47467070T>C , CM000675.1:g.47467070T>C GRCh37
NC_000013.9:g.46365071T>C NCBI36
NG_013011.1:g.9100A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000542664.4:c.413-345A>G MANE Select ENSP00000437737.1:p.=
ENST00000543956.5:c.-77-345A>G ENSP00000441861.2:p.=
ENST00000378688.8:c.413-345A>G ENSP00000367959.3:p.=
ENST00000542664.3:c.413-345A>G ENSP00000437737.1:p.=
ENST00000543956.4:c.161-345A>G ENSP00000441861.1:p.=
NM_000621.4:c.413-345A>G NP_000612.1:p.=
NM_001165947.2:c.161-345A>G NP_001159419.1:p.=
NM_000621.5:c.413-345A>G MANE Select NP_000612.1:p.=
NM_001165947.5:c.-77-345A>G NP_001159419.2:p.=
NM_001378924.1:c.413-345A>G NP_001365853.1:p.=