Canonical Allele Identifier: CA365058025
Gene: HTR1E HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.87015900G>A , CM000668.2:g.87015900G>A GRCh38
NC_000006.11:g.87725618G>A , CM000668.1:g.87725618G>A GRCh37
NC_000006.10:g.87782337G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305344.7:c.566G>A MANE Select ENSP00000307766.4:p.Gly189Asp
ENST00000305344.6:c.566G>A ENSP00000307766.4:p.Gly189Asp
NM_000865.2:c.566G>A NP_000856.1:p.Gly189Asp
XM_011535789.1:c.566G>A XP_011534091.1:p.Gly189Asp
XM_011535790.1:c.566G>A XP_011534092.1:p.Gly189Asp
XM_011535789.2:c.566G>A XP_011534091.1:p.Gly189Asp
NM_000865.3:c.566G>A MANE Select NP_000856.1:p.Gly189Asp