Canonical Allele Identifier: CA698547165
Gene: HTR2A HGNC NCBI

Linked Data

dbSNP Id: rs1164402486

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46897252G>A , CM000675.2:g.46897252G>A GRCh38
NC_000013.10:g.47471387G>A , CM000675.1:g.47471387G>A GRCh37
NC_000013.9:g.46369388G>A NCBI36
NG_013011.1:g.4783C>T

Transcript Alleles

HGVS Amino-acid change
NM_001378924.1:c.-329+700C>T NP_001365853.1:n.-329+700C>T