Canonical Allele Identifier: CA249263566
Gene: HTR2A HGNC NCBI

Linked Data

dbSNP Id: rs984926172
MyVariant Identifiers: chr13:g.46897352C>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46897352C>A , CM000675.2:g.46897352C>A GRCh38
NC_000013.10:g.47471487C>A , CM000675.1:g.47471487C>A GRCh37
NC_000013.9:g.46369488C>A NCBI36
NG_013011.1:g.4683G>T

Transcript Alleles

HGVS Amino-acid change
NM_001378924.1:c.-329+600G>T NP_001365853.1:n.-329+600G>T