Canonical Allele Identifier: CA1551421430
Gene: HTR1A HGNC NCBI

Linked Data

dbSNP Id: rs1749387649
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.63962126T>A , CM000667.2:g.63962126T>A GRCh38
NC_000005.9:g.63257953T>A , CM000667.1:g.63257953T>A GRCh37
NC_000005.8:g.63293709T>A NCBI36
NG_032816.1:g.5167A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000323865.5:c.-407A>T MANE Select ENSP00000316244.4:n.-407A>T
ENST00000323865.4:c.-407A>T ENSP00000316244.3:n.-407A>T
ENST00000506598.1:c.-387-20A>T ENSP00000423433.1:n.-387-20A>T
NM_000524.3:c.-407A>T NP_000515.2:n.-407A>T
NM_000524.4:c.-407A>T MANE Select NP_000515.2:n.-407A>T
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