Canonical Allele Identifier: CA120239642
Gene: HTR1A HGNC NCBI

Linked Data

dbSNP Id: rs186653036
gnomAD v2: 5-63258040-C-T
gnomAD v3: 5-63962213-C-T
gnomAD v4: 5-63962213-C-T
MyVariant Identifiers: chr5:g.63258040C>T (hg19) chr5:g.63962213C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.63962213C>T , CM000667.2:g.63962213C>T GRCh38
NC_000005.9:g.63258040C>T , CM000667.1:g.63258040C>T GRCh37
NC_000005.8:g.63293796C>T NCBI36
NG_032816.1:g.5080G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000323865.5:c.-494G>A MANE Select ENSP00000316244.4:n.-494G>A
ENST00000506598.1:c.-387-107G>A ENSP00000423433.1:n.-387-107G>A
NM_000524.3:c.-494G>A NP_000515.2:n.-494G>A
NM_000524.4:c.-494G>A MANE Select NP_000515.2:n.-494G>A
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