Canonical Allele Identifier: CA365057951

Gene: HTR1E

Linked Data

• dbSNP Id: rs1768315962
• MyVariant Identifiers: chr6:g.87725585A>G (hg19) ; chr6:g.87015867A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.87015867A>G , CM000668.2:g.87015867A>G	GRCh38
NC_000006.11:g.87725585A>G , CM000668.1:g.87725585A>G	GRCh37
NC_000006.10:g.87782304A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000305344.7:c.533A>G MANE Select	ENSP00000307766.4:p.Asp178Gly
ENST00000305344.6:c.533A>G	ENSP00000307766.4:p.Asp178Gly
NM_000865.2:c.533A>G	NP_000856.1:p.Asp178Gly
XM_011535789.1:c.533A>G	XP_011534091.1:p.Asp178Gly
XM_011535790.1:c.533A>G	XP_011534092.1:p.Asp178Gly
XM_011535789.2:c.533A>G	XP_011534091.1:p.Asp178Gly
NM_000865.3:c.533A>G MANE Select	NP_000856.1:p.Asp178Gly