Canonical Allele Identifier: CA13844405
Gene: HTR2A HGNC NCBI
MyVariant.info:
GRCh38 chr13:g.46897343C>T
GRCh37 chr13:g.47471478C>T
gnomAD v2:
13:47471478 C / T
gnomAD v3:
13:46897343 C / T
gnomAD v4:
chr13-46897343-C-T
Joint Max Group AF 0.56986325 (EAS)
Genomes Max Group AF 0.56986325 (EAS)
ClinVar Allele:
504813
ClinVar RCV:
RCV000605277
RCV001093594
RCV001836848
ClinVar Variation:
511090
dbSNP:
6311
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46897343C>T , CM000675.2:g.46897343C>T GRCh38
NC_000013.10:g.47471478C>T , CM000675.1:g.47471478C>T GRCh37
NC_000013.9:g.46369479C>T NCBI36
NG_013011.1:g.4692G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001378924.1:c.-329+609G>A NP_001365853.1:n.-329+609G>A
Search 100 bp 5'
Search 100 bp 3'