Canonical Allele Identifier: CA1551420499
Gene: HTR1A HGNC NCBI

Linked Data

dbSNP Id: rs1288615672

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.63960131A>C , CM000667.2:g.63960131A>C GRCh38
NC_000005.9:g.63255958A>C , CM000667.1:g.63255958A>C GRCh37
NC_000005.8:g.63291714A>C NCBI36
NG_032816.1:g.7162T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000323865.5:c.*320T>G MANE Select ENSP00000316244.4:n.*320T>G
NM_000524.3:c.*320T>G NP_000515.2:n.*320T>G
NM_000524.4:c.*320T>G MANE Select NP_000515.2:n.*320T>G