Canonical Allele Identifier: CA365057933
Gene: HTR1E HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.87725578C>G (hg19) chr6:g.87015860C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.87015860C>G , CM000668.2:g.87015860C>G GRCh38
NC_000006.11:g.87725578C>G , CM000668.1:g.87725578C>G GRCh37
NC_000006.10:g.87782297C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000305344.7:c.526C>G MANE Select ENSP00000307766.4:p.Gln176Glu
ENST00000305344.6:c.526C>G ENSP00000307766.4:p.Gln176Glu
NM_000865.2:c.526C>G NP_000856.1:p.Gln176Glu
XM_011535789.1:c.526C>G XP_011534091.1:p.Gln176Glu
XM_011535790.1:c.526C>G XP_011534092.1:p.Gln176Glu
XM_011535789.2:c.526C>G XP_011534091.1:p.Gln176Glu
NM_000865.3:c.526C>G MANE Select NP_000856.1:p.Gln176Glu
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