Canonical Allele Identifier: CA3913254

Gene: HTR1E

Linked Data

• dbSNP Id: rs764631845
• ExAC: 6:87725490 C / A
• gnomAD v2: 6-87725490-C-A
• gnomAD v4: 6-87015772-C-A
• MyVariant Identifiers: chr6:g.87725490C>A (hg19) ; chr6:g.87015772C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.87015772C>A , CM000668.2:g.87015772C>A	GRCh38
NC_000006.11:g.87725490C>A , CM000668.1:g.87725490C>A	GRCh37
NC_000006.10:g.87782209C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305344.7:c.438C>A MANE Select	ENSP00000307766.4:p.Val146=
ENST00000305344.6:c.438C>A	ENSP00000307766.4:p.Val146=
NM_000865.2:c.438C>A	NP_000856.1:p.Val146=
XM_011535789.1:c.438C>A	XP_011534091.1:p.Val146=
XM_011535790.1:c.438C>A	XP_011534092.1:p.Val146=
XM_011535789.2:c.438C>A	XP_011534091.1:p.Val146=
NM_000865.3:c.438C>A MANE Select	NP_000856.1:p.Val146=