Canonical Allele Identifier: CA388154764
Gene: HTR2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46895765C>A , CM000675.2:g.46895765C>A GRCh38
NC_000013.10:g.47469900C>A , CM000675.1:g.47469900C>A GRCh37
NC_000013.9:g.46367901C>A NCBI36
NG_013011.1:g.6270G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000542664.4:c.142G>T MANE Select ENSP00000437737.1:p.Asp48Tyr
ENST00000543956.5:c.-78+909G>T ENSP00000441861.2:n.-78+909G>T
ENST00000378688.8:c.142G>T ENSP00000367959.3:p.Asp48Tyr
ENST00000542664.3:c.142G>T ENSP00000437737.1:p.Asp48Tyr
ENST00000543956.4:c.160+909G>T ENSP00000441861.1:n.160+909G>T
ENST00000612998.1:c.49G>T ENSP00000482708.1:p.Asp17Tyr
NM_000621.4:c.142G>T NP_000612.1:p.Asp48Tyr
NM_001165947.2:c.160+909G>T NP_001159419.1:n.160+909G>T
NM_000621.5:c.142G>T MANE Select NP_000612.1:p.Asp48Tyr
NM_001165947.5:c.-78+909G>T NP_001159419.2:n.-78+909G>T
NM_001378924.1:c.142G>T NP_001365853.1:p.Asp48Tyr