Canonical Allele Identifier: CA813042891
Gene: HTR1A HGNC NCBI

Linked Data

dbSNP Id: rs1403048860
gnomAD v3: 5-63960120-A-G
gnomAD v4: 5-63960120-A-G
MyVariant Identifiers: chr5:g.63255947A>G (hg19) chr5:g.63960120A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.63960120A>G , CM000667.2:g.63960120A>G GRCh38
NC_000005.9:g.63255947A>G , CM000667.1:g.63255947A>G GRCh37
NC_000005.8:g.63291703A>G NCBI36
NG_032816.1:g.7173T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000323865.5:c.*331T>C MANE Select ENSP00000316244.4:n.*331T>C
NM_000524.3:c.*331T>C NP_000515.2:n.*331T>C
NM_000524.4:c.*331T>C MANE Select NP_000515.2:n.*331T>C
Search 100 bp 5'
Search 100 bp 3'