Canonical Allele Identifier: CA365057758
Gene: HTR1E HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.87725494A>C (hg19) chr6:g.87015776A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.87015776A>C , CM000668.2:g.87015776A>C GRCh38
NC_000006.11:g.87725494A>C , CM000668.1:g.87725494A>C GRCh37
NC_000006.10:g.87782213A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305344.7:c.442A>C MANE Select ENSP00000307766.4:p.Thr148Pro
ENST00000305344.6:c.442A>C ENSP00000307766.4:p.Thr148Pro
NM_000865.2:c.442A>C NP_000856.1:p.Thr148Pro
XM_011535789.1:c.442A>C XP_011534091.1:p.Thr148Pro
XM_011535790.1:c.442A>C XP_011534092.1:p.Thr148Pro
XM_011535789.2:c.442A>C XP_011534091.1:p.Thr148Pro
NM_000865.3:c.442A>C MANE Select NP_000856.1:p.Thr148Pro
Search 100 bp 5'
Search 100 bp 3'