Canonical Allele Identifier: CA388154689
Gene: HTR2A HGNC NCBI

Linked Data

dbSNP Id: rs1403980207

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46895731C>G , CM000675.2:g.46895731C>G GRCh38
NC_000013.10:g.47469866C>G , CM000675.1:g.47469866C>G GRCh37
NC_000013.9:g.46367867C>G NCBI36
NG_013011.1:g.6304G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000542664.4:c.176G>C MANE Select ENSP00000437737.1:p.Gly59Ala
ENST00000543956.5:c.-78+943G>C ENSP00000441861.2:n.-78+943G>C
ENST00000378688.8:c.176G>C ENSP00000367959.3:p.Gly59Ala
ENST00000542664.3:c.176G>C ENSP00000437737.1:p.Gly59Ala
ENST00000543956.4:c.160+943G>C ENSP00000441861.1:n.160+943G>C
ENST00000612998.1:c.83G>C ENSP00000482708.1:p.Gly28Ala
NM_000621.4:c.176G>C NP_000612.1:p.Gly59Ala
NM_001165947.2:c.160+943G>C NP_001159419.1:n.160+943G>C
NM_000621.5:c.176G>C MANE Select NP_000612.1:p.Gly59Ala
NM_001165947.5:c.-78+943G>C NP_001159419.2:n.-78+943G>C
NM_001378924.1:c.176G>C NP_001365853.1:p.Gly59Ala