Canonical Allele Identifier: CA1425846989
Gene: HTR3C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184060157G= , CM000665.2:g.184060157G= GRCh38
NC_000003.11:g.183777945G= , CM000665.1:g.183777945G= GRCh37
NC_000003.10:g.185260639G= NCBI36
NG_012749.1:g.12111G=

Transcript Alleles

HGVS Amino-acid change
ENST00000318351.2:c.1149G= MANE Select ENSP00000322617.1:p.Lys383=
ENST00000318351.1:c.1149G= ENSP00000322617.1:p.Lys383=
NM_130770.2:c.1149G= NP_570126.2:p.Lys383=
NM_130770.3:c.1149G= MANE Select NP_570126.2:p.Lys383=