Canonical Allele Identifier: CA451355117
Gene: HTR1E HGNC NCBI

Linked Data

COSMIC: COSM4425263
MyVariant Identifiers: chr6:g.87725679C>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.87015961C>T , CM000668.2:g.87015961C>T GRCh38
NC_000006.11:g.87725679C>T , CM000668.1:g.87725679C>T GRCh37
NC_000006.10:g.87782398C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305344.7:c.627C>T MANE Select ENSP00000307766.4:p.Ala209=
ENST00000305344.6:c.627C>T ENSP00000307766.4:p.Ala209=
NM_000865.2:c.627C>T NP_000856.1:p.Ala209=
XM_011535789.1:c.627C>T XP_011534091.1:p.Ala209=
XM_011535790.1:c.627C>T XP_011534092.1:p.Ala209=
XM_011535789.2:c.627C>T XP_011534091.1:p.Ala209=
NM_000865.3:c.627C>T MANE Select NP_000856.1:p.Ala209=
Search 100 bp 5'
Search 100 bp 3'