Canonical Allele Identifier: CA355379318
Gene: HTR3C HGNC NCBI

Linked Data

dbSNP Id: rs1368086828

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184060155A>G , CM000665.2:g.184060155A>G GRCh38
NC_000003.11:g.183777943A>G , CM000665.1:g.183777943A>G GRCh37
NC_000003.10:g.185260637A>G NCBI36
NG_012749.1:g.12109A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000318351.2:c.1147A>G MANE Select ENSP00000322617.1:p.Lys383Glu
ENST00000318351.1:c.1147A>G ENSP00000322617.1:p.Lys383Glu
NM_130770.2:c.1147A>G NP_570126.2:p.Lys383Glu
NM_130770.3:c.1147A>G MANE Select NP_570126.2:p.Lys383Glu