Canonical Allele Identifier: CA955693800
Gene: HTR2A HGNC NCBI

Linked Data

dbSNP Id: rs1950775872

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46861200_46861201del , CM000675.2:g.46861200_46861201del GRCh38
NC_000013.10:g.47435335_47435336del , CM000675.1:g.47435335_47435336del GRCh37
NC_000013.9:g.46333336_46333337del NCBI36
NG_013011.1:g.40836_40837del

Transcript Alleles

HGVS Amino-acid change
ENST00000542664.4:c.614-25560_614-25559del MANE Select ENSP00000437737.1:n.614-25560_614-25559de...
ENST00000543956.5:c.125-25560_125-25559del ENSP00000441861.2:n.125-25560_125-25559de...
ENST00000378688.8:c.614-25560_614-25559del ENSP00000367959.3:n.614-25560_614-25559de...
ENST00000542664.3:c.614-25560_614-25559del ENSP00000437737.1:n.614-25560_614-25559de...
ENST00000543956.4:c.362-25560_362-25559del ENSP00000441861.1:n.362-25560_362-25559de...
NM_000621.4:c.614-25560_614-25559del NP_000612.1:n.614-25560_614-25559del
NM_001165947.2:c.362-25560_362-25559del NP_001159419.1:n.362-25560_362-25559del
NM_000621.5:c.614-25560_614-25559del MANE Select NP_000612.1:n.614-25560_614-25559del
NM_001165947.5:c.125-25560_125-25559del NP_001159419.2:n.125-25560_125-25559del
NM_001378924.1:c.614-25560_614-25559del NP_001365853.1:n.614-25560_614-25559del