Canonical Allele Identifier: CA2725743
Gene: HTR3C HGNC NCBI

Linked Data

dbSNP Id: rs780603414
ExAC: 3:183777881 A / T
gnomAD v2: 3-183777881-A-T
gnomAD v4: 3-184060093-A-T
MyVariant Identifiers: chr3:g.183777881A>T (hg19) chr3:g.184060093A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184060093A>T , CM000665.2:g.184060093A>T GRCh38
NC_000003.11:g.183777881A>T , CM000665.1:g.183777881A>T GRCh37
NC_000003.10:g.185260575A>T NCBI36
NG_012749.1:g.12047A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000318351.2:c.1141+50A>T MANE Select ENSP00000322617.1:n.1141+50A>T
ENST00000318351.1:c.1141+50A>T ENSP00000322617.1:n.1141+50A>T
NM_130770.2:c.1141+50A>T NP_570126.2:n.1141+50A>T
NM_130770.3:c.1141+50A>T MANE Select NP_570126.2:n.1141+50A>T
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