Canonical Allele Identifier: CA120239445
Gene: HTR1A HGNC NCBI

Linked Data

dbSNP Id: rs796592086
gnomAD v2: 5-63255976-A-T
gnomAD v3: 5-63960149-A-T
gnomAD v4: 5-63960149-A-T
MyVariant Identifiers: chr5:g.63255976A>T (hg19) chr5:g.63960149A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.63960149A>T , CM000667.2:g.63960149A>T GRCh38
NC_000005.9:g.63255976A>T , CM000667.1:g.63255976A>T GRCh37
NC_000005.8:g.63291732A>T NCBI36
NG_032816.1:g.7144T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000323865.5:c.*302T>A MANE Select ENSP00000316244.4:n.*302T>A
NM_000524.3:c.*302T>A NP_000515.2:n.*302T>A
NM_000524.4:c.*302T>A MANE Select NP_000515.2:n.*302T>A
Search 100 bp 5'
Search 100 bp 3'