Canonical Allele Identifier: CA334655860

Gene: HTR2C

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.114765807T>C , CM000685.2:g.114765807T>C	GRCh38
NG_012082.2:g.186723T>C
NG_012082.3:g.186723T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276198.6:c.349+34200T>C MANE Select	ENSP00000276198.1:n.349+34200T>C
ENST00000276198.5:c.349+34200T>C	ENSP00000276198.1:n.349+34200T>C
ENST00000371950.3:c.349+34200T>C	ENSP00000361018.3:n.349+34200T>C
ENST00000371951.5:c.349+34200T>C	ENSP00000361019.1:n.349+34200T>C
NM_000868.3:c.349+34200T>C	NP_000859.1:n.349+34200T>C
NM_001256760.2:c.349+34200T>C	NP_001243689.1:n.349+34200T>C
NM_001256761.2:c.349+34200T>C	NP_001243690.1:n.349+34200T>C
XR_944300.1:n.208+23536A>G
XR_944301.1:n.208+23536A>G
XR_001755943.1:n.208+23536A>G
NM_000868.4:c.349+34200T>C MANE Select	NP_000859.2:n.349+34200T>C
NM_001256760.3:c.349+34200T>C	NP_001243689.2:n.349+34200T>C
NM_001256761.3:c.349+34200T>C	NP_001243690.2:n.349+34200T>C