Canonical Allele Identifier: CA1551420541
Gene: HTR1A HGNC NCBI

Linked Data

dbSNP Id: rs1746395478

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.63960198G>A , CM000667.2:g.63960198G>A GRCh38
NC_000005.9:g.63256025G>A , CM000667.1:g.63256025G>A GRCh37
NC_000005.8:g.63291781G>A NCBI36
NG_032816.1:g.7095C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000323865.5:c.*253C>T MANE Select ENSP00000316244.4:n.*253C>T
NM_000524.3:c.*253C>T NP_000515.2:n.*253C>T
NM_000524.4:c.*253C>T MANE Select NP_000515.2:n.*253C>T