Canonical Allele Identifier: CA3913280
Gene: HTR1E HGNC NCBI

Linked Data

dbSNP Id: rs146708836
gnomAD v2: 6-87725613-G-A
gnomAD v3: 6-87015895-G-A
gnomAD v4: 6-87015895-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.87015895G>A , CM000668.2:g.87015895G>A GRCh38
NC_000006.11:g.87725613G>A , CM000668.1:g.87725613G>A GRCh37
NC_000006.10:g.87782332G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305344.7:c.561G>A MANE Select ENSP00000307766.4:p.Thr187=
ENST00000305344.6:c.561G>A ENSP00000307766.4:p.Thr187=
NM_000865.2:c.561G>A NP_000856.1:p.Thr187=
XM_011535789.1:c.561G>A XP_011534091.1:p.Thr187=
XM_011535790.1:c.561G>A XP_011534092.1:p.Thr187=
XM_011535789.2:c.561G>A XP_011534091.1:p.Thr187=
NM_000865.3:c.561G>A MANE Select NP_000856.1:p.Thr187=