Canonical Allele Identifier: CA13918077
Gene: HTR2A HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs7322347

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46835968T>A , CM000675.2:g.46835968T>A GRCh38
NC_000013.10:g.47410103T>A , CM000675.1:g.47410103T>A GRCh37
NC_000013.9:g.46308104T>A NCBI36
NG_013011.1:g.66067A>T

Transcript Alleles

HGVS Amino-acid change
NM_000621.4:c.614-329A>T VV NP_000612.1:p.=
NM_001165947.2:c.362-329A>T VV NP_001159419.1:p.=
ENST00000378688.8:c.614-329A>T ENSP00000367959.3:p.=
ENST00000542664.3:c.614-329A>T ENSP00000437737.1:p.=
ENST00000543956.4:c.362-329A>T ENSP00000441861.1:p.=