Canonical Allele Identifier: CA3913255
Gene: HTR1E HGNC NCBI

Linked Data

dbSNP Id: rs754167574
ExAC: 6:87725498 T / A
gnomAD v2: 6-87725498-T-A
gnomAD v4: 6-87015780-T-A
MyVariant Identifiers: chr6:g.87725498T>A (hg19) chr6:g.87015780T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.87015780T>A , CM000668.2:g.87015780T>A GRCh38
NC_000006.11:g.87725498T>A , CM000668.1:g.87725498T>A GRCh37
NC_000006.10:g.87782217T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305344.7:c.446T>A MANE Select ENSP00000307766.4:p.Ile149Asn
ENST00000305344.6:c.446T>A ENSP00000307766.4:p.Ile149Asn
NM_000865.2:c.446T>A NP_000856.1:p.Ile149Asn
XM_011535789.1:c.446T>A XP_011534091.1:p.Ile149Asn
XM_011535790.1:c.446T>A XP_011534092.1:p.Ile149Asn
XM_011535789.2:c.446T>A XP_011534091.1:p.Ile149Asn
NM_000865.3:c.446T>A MANE Select NP_000856.1:p.Ile149Asn
Search 100 bp 5'
Search 100 bp 3'