Canonical Allele Identifier: CA671945393
Gene: HTR3A HGNC NCBI

Linked Data

dbSNP Id: rs1413122233
gnomAD v3: 11-113974916-C-T
gnomAD v4: 11-113974916-C-T
MyVariant Identifiers: chr11:g.113845638C>T (hg19) chr11:g.113974916C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113974916C>T , CM000673.2:g.113974916C>T GRCh38
NC_000011.9:g.113845638C>T , CM000673.1:g.113845638C>T GRCh37
NC_000011.8:g.113350848C>T NCBI36
NG_013058.1:g.4842C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000504030.6:c.-410C>T ENSP00000424189.2:n.-410C>T
Search 100 bp 5'
Search 100 bp 3'