Canonical Allele Identifier: CA813042938
Gene: HTR1A HGNC NCBI

Linked Data

dbSNP Id: rs1323926463
gnomAD v3: 5-63960217-C-T
gnomAD v4: 5-63960217-C-T
MyVariant Identifiers: chr5:g.63256044C>T (hg19) chr5:g.63960217C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.63960217C>T , CM000667.2:g.63960217C>T GRCh38
NC_000005.9:g.63256044C>T , CM000667.1:g.63256044C>T GRCh37
NC_000005.8:g.63291800C>T NCBI36
NG_032816.1:g.7076G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000323865.5:c.*234G>A MANE Select ENSP00000316244.4:n.*234G>A
NM_000524.3:c.*234G>A NP_000515.2:n.*234G>A
NM_000524.4:c.*234G>A MANE Select NP_000515.2:n.*234G>A
Search 100 bp 5'
Search 100 bp 3'