Canonical Allele Identifier: CA560082682
Gene: HTR1A HGNC NCBI

Linked Data

dbSNP Id: rs1389148340
gnomAD v2: 5-63255927-C-T
gnomAD v3: 5-63960100-C-T
gnomAD v4: 5-63960100-C-T
MyVariant Identifiers: chr5:g.63255927C>T (hg19) chr5:g.63960100C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.63960100C>T , CM000667.2:g.63960100C>T GRCh38
NC_000005.9:g.63255927C>T , CM000667.1:g.63255927C>T GRCh37
NC_000005.8:g.63291683C>T NCBI36
NG_032816.1:g.7193G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000323865.5:c.*351G>A MANE Select ENSP00000316244.4:n.*351G>A
NM_000524.3:c.*351G>A NP_000515.2:n.*351G>A
NM_000524.4:c.*351G>A MANE Select NP_000515.2:n.*351G>A
Search 100 bp 5'
Search 100 bp 3'