Canonical Allele Identifier: CA365057946
Gene: HTR1E HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.87725583C>A (hg19) chr6:g.87015865C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.87015865C>A , CM000668.2:g.87015865C>A GRCh38
NC_000006.11:g.87725583C>A , CM000668.1:g.87725583C>A GRCh37
NC_000006.10:g.87782302C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000305344.7:c.531C>A MANE Select ENSP00000307766.4:p.His177Gln
ENST00000305344.6:c.531C>A ENSP00000307766.4:p.His177Gln
NM_000865.2:c.531C>A NP_000856.1:p.His177Gln
XM_011535789.1:c.531C>A XP_011534091.1:p.His177Gln
XM_011535790.1:c.531C>A XP_011534092.1:p.His177Gln
XM_011535789.2:c.531C>A XP_011534091.1:p.His177Gln
NM_000865.3:c.531C>A MANE Select NP_000856.1:p.His177Gln
Search 100 bp 5'
Search 100 bp 3'