Canonical Allele Identifier: CA365058166
Gene: HTR1E HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000305344.7:c.632G>C MANE Select ENSP00000307766.4:p.Ser211Thr
ENST00000305344.6:c.632G>C ENSP00000307766.4:p.Ser211Thr
NM_000865.2:c.632G>C NP_000856.1:p.Ser211Thr
XM_011535789.1:c.632G>C XP_011534091.1:p.Ser211Thr
XM_011535790.1:c.632G>C XP_011534092.1:p.Ser211Thr
XM_011535789.2:c.632G>C XP_011534091.1:p.Ser211Thr
NM_000865.3:c.632G>C MANE Select NP_000856.1:p.Ser211Thr