Canonical Allele Identifier: CA214531
Gene: HTR5A HGNC NCBI
HTR5A-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 161768
ClinVar RCV Id: RCV000149304
dbSNP Id: rs193920930
ExAC: 7:154862688 G / C
gnomAD v2: 7-154862688-G-C
gnomAD v4: 7-155070978-G-C
COSMIC: COSM1180172
MyVariant Identifiers: chr7:g.154862688G>C (hg19) chr7:g.155070978G>C (hg38)
PubMed: PMID:23265383
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.155070978G>C , CM000669.2:g.155070978G>C GRCh38
NC_000007.13:g.154862688G>C , CM000669.1:g.154862688G>C GRCh37
NC_000007.12:g.154493621G>C NCBI36
NG_044997.1:g.5655G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000287907.3:c.79G>C (HTR5A) MANE Select ENSP00000287907.2:p.Asp27His
ENST00000287907.2:c.79G>C (HTR5A) ENSP00000287907.2:p.Asp27His
NM_024012.3:c.79G>C (HTR5A) NP_076917.1:p.Asp27His
NR_038945.1:n.524+56C>G (HTR5A-AS1)
NM_024012.4:c.79G>C (HTR5A) MANE Select NP_076917.1:p.Asp27His
Search 100 bp 5'
Search 100 bp 3'