Canonical Allele Identifier: CA355380047
Gene: HTR3C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184060303T>G , CM000665.2:g.184060303T>G GRCh38
NC_000003.11:g.183778091T>G , CM000665.1:g.183778091T>G GRCh37
NC_000003.10:g.185260785T>G NCBI36
NG_012749.1:g.12257T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000318351.2:c.1295T>G MANE Select ENSP00000322617.1:p.Leu432Arg
ENST00000318351.1:c.1295T>G ENSP00000322617.1:p.Leu432Arg
NM_130770.2:c.1295T>G NP_570126.2:p.Leu432Arg
NM_130770.3:c.1295T>G MANE Select NP_570126.2:p.Leu432Arg