Canonical Allele Identifier: CA3913268
Gene: HTR1E HGNC NCBI

Linked Data

dbSNP Id: rs373132619
ExAC: 6:87725546 G / A
gnomAD v2: 6-87725546-G-A
gnomAD v3: 6-87015828-G-A
gnomAD v4: 6-87015828-G-A
MyVariant Identifiers: chr6:g.87725546G>A (hg19) chr6:g.87015828G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.87015828G>A , CM000668.2:g.87015828G>A GRCh38
NC_000006.11:g.87725546G>A , CM000668.1:g.87725546G>A GRCh37
NC_000006.10:g.87782265G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305344.7:c.494G>A MANE Select ENSP00000307766.4:p.Arg165His
ENST00000305344.6:c.494G>A ENSP00000307766.4:p.Arg165His
NM_000865.2:c.494G>A NP_000856.1:p.Arg165His
XM_011535789.1:c.494G>A XP_011534091.1:p.Arg165His
XM_011535790.1:c.494G>A XP_011534092.1:p.Arg165His
XM_011535789.2:c.494G>A XP_011534091.1:p.Arg165His
NM_000865.3:c.494G>A MANE Select NP_000856.1:p.Arg165His
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