Canonical Allele Identifier: CA609569551
Gene: HTR2A HGNC NCBI

Linked Data

dbSNP Id: rs1341540652
gnomAD v2: 13-47471220-CTA-C
gnomAD v3: 13-46897085-CTA-C
gnomAD v4: 13-46897085-CTA-C
MyVariant Identifiers: chr13:g.47471221_47471222del (hg19) chr13:g.46897086_46897087del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46897087_46897088del , CM000675.2:g.46897087_46897088del GRCh38
NC_000013.10:g.47471222_47471223del , CM000675.1:g.47471222_47471223del GRCh37
NC_000013.9:g.46369223_46369224del NCBI36
NG_013011.1:g.4948_4949del

Transcript Alleles

HGVS Amino-acid Change
NM_001378924.1:c.-328-853_-328-852del NP_001365853.1:n.-328-853_-328-852del
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