Canonical Allele Identifier: CA365057836
Gene: HTR1E HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.87725531G>A (hg19) chr6:g.87015813G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.87015813G>A , CM000668.2:g.87015813G>A GRCh38
NC_000006.11:g.87725531G>A , CM000668.1:g.87725531G>A GRCh37
NC_000006.10:g.87782250G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305344.7:c.479G>A MANE Select ENSP00000307766.4:p.Trp160Ter
ENST00000305344.6:c.479G>A ENSP00000307766.4:p.Trp160Ter
NM_000865.2:c.479G>A NP_000856.1:p.Trp160Ter
XM_011535789.1:c.479G>A XP_011534091.1:p.Trp160Ter
XM_011535790.1:c.479G>A XP_011534092.1:p.Trp160Ter
XM_011535789.2:c.479G>A XP_011534091.1:p.Trp160Ter
NM_000865.3:c.479G>A MANE Select NP_000856.1:p.Trp160Ter
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