Canonical Allele Identifier: CA2725777
Gene: HTR3C HGNC NCBI

Linked Data

dbSNP Id: rs143741187
ExAC: 3:183778031 T / C
gnomAD v2: 3-183778031-T-C
gnomAD v3: 3-184060243-T-C
gnomAD v4: 3-184060243-T-C
MyVariant Identifiers: chr3:g.183778031T>C (hg19) chr3:g.184060243T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184060243T>C , CM000665.2:g.184060243T>C GRCh38
NC_000003.11:g.183778031T>C , CM000665.1:g.183778031T>C GRCh37
NC_000003.10:g.185260725T>C NCBI36
NG_012749.1:g.12197T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000318351.2:c.1235T>C MANE Select ENSP00000322617.1:p.Met412Thr
ENST00000318351.1:c.1235T>C ENSP00000322617.1:p.Met412Thr
NM_130770.2:c.1235T>C NP_570126.2:p.Met412Thr
NM_130770.3:c.1235T>C MANE Select NP_570126.2:p.Met412Thr
Search 100 bp 5'
Search 100 bp 3'