Canonical Allele Identifier: CA437322469
Gene: HTR3C HGNC NCBI

Linked Data

dbSNP Id: rs1250795913
gnomAD v2: 3-183777827-G-A
gnomAD v4: 3-184060039-G-A
MyVariant Identifiers: chr3:g.183777827G>A (hg19) chr3:g.184060039G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184060039G>A , CM000665.2:g.184060039G>A GRCh38
NC_000003.11:g.183777827G>A , CM000665.1:g.183777827G>A GRCh37
NC_000003.10:g.185260521G>A NCBI36
NG_012749.1:g.11993G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000318351.2:c.1137G>A MANE Select ENSP00000322617.1:p.Leu379=
ENST00000318351.1:c.1137G>A ENSP00000322617.1:p.Leu379=
NM_130770.2:c.1137G>A NP_570126.2:p.Leu379=
NM_130770.3:c.1137G>A MANE Select NP_570126.2:p.Leu379=
Search 100 bp 5'
Search 100 bp 3'