Canonical Allele Identifier: CA365058157

Gene: HTR1E

Linked Data

• gnomAD v4: 6-87015962-A-G
• MyVariant Identifiers: chr6:g.87725680A>G (hg19) ; chr6:g.87015962A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.87015962A>G , CM000668.2:g.87015962A>G	GRCh38
NC_000006.11:g.87725680A>G , CM000668.1:g.87725680A>G	GRCh37
NC_000006.10:g.87782399A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305344.7:c.628A>G MANE Select	ENSP00000307766.4:p.Lys210Glu
ENST00000305344.6:c.628A>G	ENSP00000307766.4:p.Lys210Glu
NM_000865.2:c.628A>G	NP_000856.1:p.Lys210Glu
XM_011535789.1:c.628A>G	XP_011534091.1:p.Lys210Glu
XM_011535790.1:c.628A>G	XP_011534092.1:p.Lys210Glu
XM_011535789.2:c.628A>G	XP_011534091.1:p.Lys210Glu
NM_000865.3:c.628A>G MANE Select	NP_000856.1:p.Lys210Glu