Canonical Allele Identifier: CA548793711

Gene: HTR3C

Linked Data

• dbSNP Id: rs1392592830
• gnomAD v2: 3-183777928-C-T
• gnomAD v3: 3-184060140-C-T
• gnomAD v4: 3-184060140-C-T
• MyVariant Identifiers: chr3:g.183777928C>T (hg19) ; chr3:g.184060140C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184060140C>T , CM000665.2:g.184060140C>T	GRCh38
NC_000003.11:g.183777928C>T , CM000665.1:g.183777928C>T	GRCh37
NC_000003.10:g.185260622C>T	NCBI36
NG_012749.1:g.12094C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000318351.2:c.1142-10C>T MANE Select	ENSP00000322617.1:n.1142-10C>T
ENST00000318351.1:c.1142-10C>T	ENSP00000322617.1:n.1142-10C>T
NM_130770.2:c.1142-10C>T	NP_570126.2:n.1142-10C>T
NM_130770.3:c.1142-10C>T MANE Select	NP_570126.2:n.1142-10C>T