Canonical Allele Identifier: CA903679454
Gene: HTR3C HGNC NCBI

Linked Data

dbSNP Id: rs1389439003
gnomAD v4: 3-184060064-C-A
MyVariant Identifiers: chr3:g.183777852C>A (hg19) chr3:g.184060064C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184060064C>A , CM000665.2:g.184060064C>A GRCh38
NC_000003.11:g.183777852C>A , CM000665.1:g.183777852C>A GRCh37
NC_000003.10:g.185260546C>A NCBI36
NG_012749.1:g.12018C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000318351.2:c.1141+21C>A MANE Select ENSP00000322617.1:n.1141+21C>A
ENST00000318351.1:c.1141+21C>A ENSP00000322617.1:n.1141+21C>A
NM_130770.2:c.1141+21C>A NP_570126.2:n.1141+21C>A
NM_130770.3:c.1141+21C>A MANE Select NP_570126.2:n.1141+21C>A
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