Canonical Allele Identifier: CA3913281
Gene: HTR1E HGNC NCBI

Linked Data

dbSNP Id: rs755175910
ExAC: 6:87725621 C / T
gnomAD v4: 6-87015903-C-T
COSMIC: COSM197760
MyVariant Identifiers: chr6:g.87725621C>T (hg19) chr6:g.87015903C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.87015903C>T , CM000668.2:g.87015903C>T GRCh38
NC_000006.11:g.87725621C>T , CM000668.1:g.87725621C>T GRCh37
NC_000006.10:g.87782340C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305344.7:c.569C>T MANE Select ENSP00000307766.4:p.Ala190Val
ENST00000305344.6:c.569C>T ENSP00000307766.4:p.Ala190Val
NM_000865.2:c.569C>T NP_000856.1:p.Ala190Val
XM_011535789.1:c.569C>T XP_011534091.1:p.Ala190Val
XM_011535790.1:c.569C>T XP_011534092.1:p.Ala190Val
XM_011535789.2:c.569C>T XP_011534091.1:p.Ala190Val
NM_000865.3:c.569C>T MANE Select NP_000856.1:p.Ala190Val
Search 100 bp 5'
Search 100 bp 3'