Canonical Allele Identifier: CA120239442
Gene: HTR1A HGNC NCBI

Linked Data

dbSNP Id: rs932975756
gnomAD v3: 5-63960134-T-C
gnomAD v4: 5-63960134-T-C
MyVariant Identifiers: chr5:g.63255961T>C (hg19) chr5:g.63960134T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.63960134T>C , CM000667.2:g.63960134T>C GRCh38
NC_000005.9:g.63255961T>C , CM000667.1:g.63255961T>C GRCh37
NC_000005.8:g.63291717T>C NCBI36
NG_032816.1:g.7159A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000323865.5:c.*317A>G MANE Select ENSP00000316244.4:n.*317A>G
NM_000524.3:c.*317A>G NP_000515.2:n.*317A>G
NM_000524.4:c.*317A>G MANE Select NP_000515.2:n.*317A>G
Search 100 bp 5'
Search 100 bp 3'