Canonical Allele Identifier: CA2725760
Gene: HTR3C HGNC NCBI

Linked Data

dbSNP Id: rs780515932
ExAC: 3:183777960 A / G
gnomAD v2: 3-183777960-A-G
gnomAD v3: 3-184060172-A-G
gnomAD v4: 3-184060172-A-G
MyVariant Identifiers: chr3:g.183777960A>G (hg19) chr3:g.184060172A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184060172A>G , CM000665.2:g.184060172A>G GRCh38
NC_000003.11:g.183777960A>G , CM000665.1:g.183777960A>G GRCh37
NC_000003.10:g.185260654A>G NCBI36
NG_012749.1:g.12126A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000318351.2:c.1164A>G MANE Select ENSP00000322617.1:p.Leu388=
ENST00000318351.1:c.1164A>G ENSP00000322617.1:p.Leu388=
NM_130770.2:c.1164A>G NP_570126.2:p.Leu388=
NM_130770.3:c.1164A>G MANE Select NP_570126.2:p.Leu388=
Search 100 bp 5'
Search 100 bp 3'