Canonical Allele Identifier: CA560082679
Gene: HTR1A HGNC NCBI

Linked Data

dbSNP Id: rs1253473957
gnomAD v2: 5-63255898-T-C
gnomAD v3: 5-63960071-T-C
gnomAD v4: 5-63960071-T-C
MyVariant Identifiers: chr5:g.63255898T>C (hg19) chr5:g.63960071T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.63960071T>C , CM000667.2:g.63960071T>C GRCh38
NC_000005.9:g.63255898T>C , CM000667.1:g.63255898T>C GRCh37
NC_000005.8:g.63291654T>C NCBI36
NG_032816.1:g.7222A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000323865.5:c.*380A>G MANE Select ENSP00000316244.4:n.*380A>G
NM_000524.3:c.*380A>G NP_000515.2:n.*380A>G
NM_000524.4:c.*380A>G MANE Select NP_000515.2:n.*380A>G
Search 100 bp 5'
Search 100 bp 3'