Canonical Allele Identifier: CA451355652

Gene: HTR1E

Linked Data

• dbSNP Id: rs1768314112
• gnomAD v4: 6-87015806-C-T
• COSMIC: COSM3630352
• MyVariant Identifiers: chr6:g.87725524C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.87015806C>T , CM000668.2:g.87015806C>T	GRCh38
NC_000006.11:g.87725524C>T , CM000668.1:g.87725524C>T	GRCh37
NC_000006.10:g.87782243C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305344.7:c.472C>T MANE Select	ENSP00000307766.4:p.Leu158=
ENST00000305344.6:c.472C>T	ENSP00000307766.4:p.Leu158=
NM_000865.2:c.472C>T	NP_000856.1:p.Leu158=
XM_011535789.1:c.472C>T	XP_011534091.1:p.Leu158=
XM_011535790.1:c.472C>T	XP_011534092.1:p.Leu158=
XM_011535789.2:c.472C>T	XP_011534091.1:p.Leu158=
NM_000865.3:c.472C>T MANE Select	NP_000856.1:p.Leu158=