Canonical Allele Identifier: CA437322996
Gene: HTR3C HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.183777794A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184060006A>C , CM000665.2:g.184060006A>C GRCh38
NC_000003.11:g.183777794A>C , CM000665.1:g.183777794A>C GRCh37
NC_000003.10:g.185260488A>C NCBI36
NG_012749.1:g.11960A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000318351.2:c.1104A>C MANE Select ENSP00000322617.1:p.Gly368=
ENST00000318351.1:c.1104A>C ENSP00000322617.1:p.Gly368=
NM_130770.2:c.1104A>C NP_570126.2:p.Gly368=
NM_130770.3:c.1104A>C MANE Select NP_570126.2:p.Gly368=