Canonical Allele Identifier: CA365058165

Gene: HTR1E

Linked Data

• MyVariant Identifiers: chr6:g.87725684G>A (hg19) ; chr6:g.87015966G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.87015966G>A , CM000668.2:g.87015966G>A	GRCh38
NC_000006.11:g.87725684G>A , CM000668.1:g.87725684G>A	GRCh37
NC_000006.10:g.87782403G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305344.7:c.632G>A MANE Select	ENSP00000307766.4:p.Ser211Asn
ENST00000305344.6:c.632G>A	ENSP00000307766.4:p.Ser211Asn
NM_000865.2:c.632G>A	NP_000856.1:p.Ser211Asn
XM_011535789.1:c.632G>A	XP_011534091.1:p.Ser211Asn
XM_011535790.1:c.632G>A	XP_011534092.1:p.Ser211Asn
XM_011535789.2:c.632G>A	XP_011534091.1:p.Ser211Asn
NM_000865.3:c.632G>A MANE Select	NP_000856.1:p.Ser211Asn