Canonical Allele Identifier: CA365057826
Gene: HTR1E HGNC NCBI

Linked Data

gnomAD v4: 6-87015809-T-C
MyVariant Identifiers: chr6:g.87725527T>C (hg19) chr6:g.87015809T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.87015809T>C , CM000668.2:g.87015809T>C GRCh38
NC_000006.11:g.87725527T>C , CM000668.1:g.87725527T>C GRCh37
NC_000006.10:g.87782246T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305344.7:c.475T>C MANE Select ENSP00000307766.4:p.Phe159Leu
ENST00000305344.6:c.475T>C ENSP00000307766.4:p.Phe159Leu
NM_000865.2:c.475T>C NP_000856.1:p.Phe159Leu
XM_011535789.1:c.475T>C XP_011534091.1:p.Phe159Leu
XM_011535790.1:c.475T>C XP_011534092.1:p.Phe159Leu
XM_011535789.2:c.475T>C XP_011534091.1:p.Phe159Leu
NM_000865.3:c.475T>C MANE Select NP_000856.1:p.Phe159Leu
Search 100 bp 5'
Search 100 bp 3'