Canonical Allele Identifier: CA365058144

Gene: HTR1E

Linked Data

• gnomAD v4: 6-87015955-C-G
• MyVariant Identifiers: chr6:g.87725673C>G (hg19) ; chr6:g.87015955C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.87015955C>G , CM000668.2:g.87015955C>G	GRCh38
NC_000006.11:g.87725673C>G , CM000668.1:g.87725673C>G	GRCh37
NC_000006.10:g.87782392C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305344.7:c.621C>G MANE Select	ENSP00000307766.4:p.His207Gln
ENST00000305344.6:c.621C>G	ENSP00000307766.4:p.His207Gln
NM_000865.2:c.621C>G	NP_000856.1:p.His207Gln
XM_011535789.1:c.621C>G	XP_011534091.1:p.His207Gln
XM_011535790.1:c.621C>G	XP_011534092.1:p.His207Gln
XM_011535789.2:c.621C>G	XP_011534091.1:p.His207Gln
NM_000865.3:c.621C>G MANE Select	NP_000856.1:p.His207Gln