Canonical Allele Identifier: CA365058170

Gene: HTR1E

Linked Data

• MyVariant Identifiers: chr6:g.87725686C>T (hg19) ; chr6:g.87015968C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.87015968C>T , CM000668.2:g.87015968C>T	GRCh38
NC_000006.11:g.87725686C>T , CM000668.1:g.87725686C>T	GRCh37
NC_000006.10:g.87782405C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305344.7:c.634C>T MANE Select	ENSP00000307766.4:p.Leu212Phe
ENST00000305344.6:c.634C>T	ENSP00000307766.4:p.Leu212Phe
NM_000865.2:c.634C>T	NP_000856.1:p.Leu212Phe
XM_011535789.1:c.634C>T	XP_011534091.1:p.Leu212Phe
XM_011535790.1:c.634C>T	XP_011534092.1:p.Leu212Phe
XM_011535789.2:c.634C>T	XP_011534091.1:p.Leu212Phe
NM_000865.3:c.634C>T MANE Select	NP_000856.1:p.Leu212Phe