Canonical Allele Identifier: CA3913264
Gene: HTR1E HGNC NCBI

Linked Data

dbSNP Id: rs777898827
ExAC: 6:87725541 C / A
gnomAD v2: 6-87725541-C-A
gnomAD v4: 6-87015823-C-A
MyVariant Identifiers: chr6:g.87725541C>A (hg19) chr6:g.87015823C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.87015823C>A , CM000668.2:g.87015823C>A GRCh38
NC_000006.11:g.87725541C>A , CM000668.1:g.87725541C>A GRCh37
NC_000006.10:g.87782260C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305344.7:c.489C>A MANE Select ENSP00000307766.4:p.His163Gln
ENST00000305344.6:c.489C>A ENSP00000307766.4:p.His163Gln
NM_000865.2:c.489C>A NP_000856.1:p.His163Gln
XM_011535789.1:c.489C>A XP_011534091.1:p.His163Gln
XM_011535790.1:c.489C>A XP_011534092.1:p.His163Gln
XM_011535789.2:c.489C>A XP_011534091.1:p.His163Gln
NM_000865.3:c.489C>A MANE Select NP_000856.1:p.His163Gln
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