Canonical Allele Identifier: CA1425846958

Gene: HTR3C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184060094C= , CM000665.2:g.184060094C=	GRCh38
NC_000003.11:g.183777882C= , CM000665.1:g.183777882C=	GRCh37
NC_000003.10:g.185260576C=	NCBI36
NG_012749.1:g.12048C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318351.2:c.1141+51C= MANE Select	ENSP00000322617.1:n.1141+51C=
ENST00000318351.1:c.1141+51C=	ENSP00000322617.1:n.1141+51C=
NM_130770.2:c.1141+51C=	NP_570126.2:n.1141+51C=
NM_130770.3:c.1141+51C= MANE Select	NP_570126.2:n.1141+51C=