Canonical Allele Identifier: CA365057924

Gene: HTR1E

Linked Data

• MyVariant Identifiers: chr6:g.87725573C>T (hg19) ; chr6:g.87015855C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.87015855C>T , CM000668.2:g.87015855C>T	GRCh38
NC_000006.11:g.87725573C>T , CM000668.1:g.87725573C>T	GRCh37
NC_000006.10:g.87782292C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305344.7:c.521C>T MANE Select	ENSP00000307766.4:p.Thr174Ile
ENST00000305344.6:c.521C>T	ENSP00000307766.4:p.Thr174Ile
NM_000865.2:c.521C>T	NP_000856.1:p.Thr174Ile
XM_011535789.1:c.521C>T	XP_011534091.1:p.Thr174Ile
XM_011535790.1:c.521C>T	XP_011534092.1:p.Thr174Ile
XM_011535789.2:c.521C>T	XP_011534091.1:p.Thr174Ile
NM_000865.3:c.521C>T MANE Select	NP_000856.1:p.Thr174Ile