Canonical Allele Identifier: CA365058164
Gene: HTR1E HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.87015965A>T , CM000668.2:g.87015965A>T GRCh38
NC_000006.11:g.87725683A>T , CM000668.1:g.87725683A>T GRCh37
NC_000006.10:g.87782402A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305344.7:c.631A>T MANE Select ENSP00000307766.4:p.Ser211Cys
ENST00000305344.6:c.631A>T ENSP00000307766.4:p.Ser211Cys
NM_000865.2:c.631A>T NP_000856.1:p.Ser211Cys
XM_011535789.1:c.631A>T XP_011534091.1:p.Ser211Cys
XM_011535790.1:c.631A>T XP_011534092.1:p.Ser211Cys
XM_011535789.2:c.631A>T XP_011534091.1:p.Ser211Cys
NM_000865.3:c.631A>T MANE Select NP_000856.1:p.Ser211Cys