Canonical Allele Identifier: CA4584887
Gene: HTR5A HGNC NCBI
HTR5A-AS1 HGNC NCBI
COSMIC:
COSM150432 (not active)
MyVariant.info:
GRCh38 chr7:g.155070911T>A
GRCh37 chr7:g.154862621T>A
gnomAD v2:
7:154862621 T / A
gnomAD v3:
7:155070911 T / A
gnomAD v4:
chr7-155070911-T-A
Joint Max Group AF 0.38249047 (EAS)
Genomes Max Group AF 0.35384039 (EAS)
Exomes Max Group AF 0.38472827 (EAS)
dbSNP:
6320
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.155070911T>A , CM000669.2:g.155070911T>A GRCh38
NC_000007.13:g.154862621T>A , CM000669.1:g.154862621T>A GRCh37
NC_000007.12:g.154493554T>A NCBI36
NG_044997.1:g.5588T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000287907.3:c.12T>A (HTR5A) MANE Select ENSP00000287907.2:p.Pro4=
ENST00000287907.2:c.12T>A (HTR5A) ENSP00000287907.2:p.Pro4=
NM_024012.3:c.12T>A (HTR5A) NP_076917.1:p.Pro4=
NR_038945.1:n.524+123A>T (HTR5A-AS1)
NM_024012.4:c.12T>A (HTR5A) MANE Select NP_076917.1:p.Pro4=
Search 100 bp 5'
Search 100 bp 3'