Canonical Allele Identifier: CA365058158
Gene: HTR1E HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.87725681A>C (hg19) chr6:g.87015963A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.87015963A>C , CM000668.2:g.87015963A>C GRCh38
NC_000006.11:g.87725681A>C , CM000668.1:g.87725681A>C GRCh37
NC_000006.10:g.87782400A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305344.7:c.629A>C MANE Select ENSP00000307766.4:p.Lys210Thr
ENST00000305344.6:c.629A>C ENSP00000307766.4:p.Lys210Thr
NM_000865.2:c.629A>C NP_000856.1:p.Lys210Thr
XM_011535789.1:c.629A>C XP_011534091.1:p.Lys210Thr
XM_011535790.1:c.629A>C XP_011534092.1:p.Lys210Thr
XM_011535789.2:c.629A>C XP_011534091.1:p.Lys210Thr
NM_000865.3:c.629A>C MANE Select NP_000856.1:p.Lys210Thr
Search 100 bp 5'
Search 100 bp 3'