Canonical Allele Identifier: CA1551420603
Gene: HTR1A HGNC NCBI

Linked Data

dbSNP Id: rs1746398466
gnomAD v4: 5-63960308-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.63960308G>A , CM000667.2:g.63960308G>A GRCh38
NC_000005.9:g.63256135G>A , CM000667.1:g.63256135G>A GRCh37
NC_000005.8:g.63291891G>A NCBI36
NG_032816.1:g.6985C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000323865.5:c.*143C>T MANE Select ENSP00000316244.4:n.*143C>T
NM_000524.3:c.*143C>T NP_000515.2:n.*143C>T
NM_000524.4:c.*143C>T MANE Select NP_000515.2:n.*143C>T