Canonical Allele Identifier: CA2728062257
Gene: HTR2A HGNC NCBI

Linked Data

dbSNP Id: rs2138262352

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46897378C>T , CM000675.2:g.46897378C>T GRCh38
NC_000013.10:g.47471513C>T , CM000675.1:g.47471513C>T GRCh37
NC_000013.9:g.46369514C>T NCBI36
NG_013011.1:g.4657G>A

Transcript Alleles

HGVS Amino-acid change
NM_001378924.1:c.-329+574G>A NP_001365853.1:n.-329+574G>A