Canonical Allele Identifier: CA355378995
Gene: HTR3C HGNC NCBI

Linked Data

dbSNP Id: rs1576990001
gnomAD v4: 3-184059995-C-A
MyVariant Identifiers: chr3:g.183777783C>A (hg19) chr3:g.184059995C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184059995C>A , CM000665.2:g.184059995C>A GRCh38
NC_000003.11:g.183777783C>A , CM000665.1:g.183777783C>A GRCh37
NC_000003.10:g.185260477C>A NCBI36
NG_012749.1:g.11949C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000318351.2:c.1093C>A MANE Select ENSP00000322617.1:p.Pro365Thr
ENST00000318351.1:c.1093C>A ENSP00000322617.1:p.Pro365Thr
NM_130770.2:c.1093C>A NP_570126.2:p.Pro365Thr
NM_130770.3:c.1093C>A MANE Select NP_570126.2:p.Pro365Thr
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