Canonical Allele Identifier: CA870275139

Gene: HTR2C

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.114584109C>A , CM000685.2:g.114584109C>A	GRCh38
NG_012082.2:g.5025C>A
NG_012082.3:g.5025C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276198.6:c.-697C>A MANE Select	ENSP00000276198.1:n.-697C>A
ENST00000276198.5:c.-697C>A	ENSP00000276198.1:n.-697C>A
ENST00000371950.3:c.-697C>A	ENSP00000361018.3:n.-697C>A
ENST00000371951.5:c.-788C>A	ENSP00000361019.1:n.-788C>A
NM_000868.3:c.-697C>A	NP_000859.1:n.-697C>A
NM_001256760.2:c.-788C>A	NP_001243689.1:n.-788C>A
NM_001256761.2:c.-697C>A	NP_001243690.1:n.-697C>A
NM_000868.4:c.-697C>A MANE Select	NP_000859.2:n.-697C>A
NM_001256760.3:c.-788C>A	NP_001243689.2:n.-788C>A
NM_001256761.3:c.-697C>A	NP_001243690.2:n.-697C>A