Canonical Allele Identifier: CA437322487
Gene: HTR3C HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.183777957G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184060169G>A , CM000665.2:g.184060169G>A GRCh38
NC_000003.11:g.183777957G>A , CM000665.1:g.183777957G>A GRCh37
NC_000003.10:g.185260651G>A NCBI36
NG_012749.1:g.12123G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000318351.2:c.1161G>A MANE Select ENSP00000322617.1:p.Glu387=
ENST00000318351.1:c.1161G>A ENSP00000322617.1:p.Glu387=
NM_130770.2:c.1161G>A NP_570126.2:p.Glu387=
NM_130770.3:c.1161G>A MANE Select NP_570126.2:p.Glu387=