Canonical Allele Identifier: CA249263411
Gene: HTR2A HGNC NCBI

Linked Data

dbSNP Id: rs539726671
gnomAD v4: 13-46897142-C-A
MyVariant Identifiers: chr13:g.47471277C>A (hg19) chr13:g.46897142C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46897142C>A , CM000675.2:g.46897142C>A GRCh38
NC_000013.10:g.47471277C>A , CM000675.1:g.47471277C>A GRCh37
NC_000013.9:g.46369278C>A NCBI36
NG_013011.1:g.4893G>T

Transcript Alleles

HGVS Amino-acid Change
NM_001378924.1:c.-329+810G>T NP_001365853.1:n.-329+810G>T
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