Canonical Allele Identifier: CA334663267

Gene: HTR2C

Linked Data

• dbSNP Id: rs782221156
• MyVariant Identifiers: chrX:g.114138220C>T (hg19) ; chrX:g.114903657C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.114903657C>T , CM000685.2:g.114903657C>T	GRCh38
NC_000023.10:g.114138220C>T , CM000685.1:g.114138220C>T	GRCh37
NC_000023.9:g.114044476C>T	NCBI36
NG_012082.2:g.324573C>T
NG_012082.3:g.324573C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000276198.6:c.551-2932C>T MANE Select	ENSP00000276198.1:n.551-2932C>T
ENST00000276198.5:c.551-2932C>T	ENSP00000276198.1:n.551-2932C>T
ENST00000371950.3:c.456-2932C>T	ENSP00000361018.3:n.456-2932C>T
ENST00000371951.5:c.551-2932C>T	ENSP00000361019.1:n.551-2932C>T
NM_000868.3:c.551-2932C>T	NP_000859.1:n.551-2932C>T
NM_001256760.2:c.551-2932C>T	NP_001243689.1:n.551-2932C>T
NM_001256761.2:c.456-2932C>T	NP_001243690.1:n.456-2932C>T
NM_000868.4:c.551-2932C>T MANE Select	NP_000859.2:n.551-2932C>T
NM_001256760.3:c.551-2932C>T	NP_001243689.2:n.551-2932C>T
NM_001256761.3:c.456-2932C>T	NP_001243690.2:n.456-2932C>T