Canonical Allele Identifier: CA1076831847
Gene: HTR1A HGNC NCBI

Linked Data

dbSNP Id: rs1746398663
gnomAD v3: 5-63960315-T-A
gnomAD v4: 5-63960315-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.63960315T>A , CM000667.2:g.63960315T>A GRCh38
NC_000005.9:g.63256142T>A , CM000667.1:g.63256142T>A GRCh37
NC_000005.8:g.63291898T>A NCBI36
NG_032816.1:g.6978A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000323865.5:c.*136A>T MANE Select ENSP00000316244.4:n.*136A>T
NM_000524.3:c.*136A>T NP_000515.2:n.*136A>T
NM_000524.4:c.*136A>T MANE Select NP_000515.2:n.*136A>T