Canonical Allele Identifier: CA143159902
Gene: HTR1E HGNC NCBI

Linked Data

dbSNP Id: rs926195051
gnomAD v4: 6-87015795-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.87015795C>G , CM000668.2:g.87015795C>G GRCh38
NC_000006.11:g.87725513C>G , CM000668.1:g.87725513C>G GRCh37
NC_000006.10:g.87782232C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305344.7:c.461C>G MANE Select ENSP00000307766.4:p.Ser154Cys
ENST00000305344.6:c.461C>G ENSP00000307766.4:p.Ser154Cys
NM_000865.2:c.461C>G NP_000856.1:p.Ser154Cys
XM_011535789.1:c.461C>G XP_011534091.1:p.Ser154Cys
XM_011535790.1:c.461C>G XP_011534092.1:p.Ser154Cys
XM_011535789.2:c.461C>G XP_011534091.1:p.Ser154Cys
NM_000865.3:c.461C>G MANE Select NP_000856.1:p.Ser154Cys