Canonical Allele Identifier: CA365057842
Gene: HTR1E HGNC NCBI

Linked Data

dbSNP Id: rs1768314282

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.87015815A>G , CM000668.2:g.87015815A>G GRCh38
NC_000006.11:g.87725533A>G , CM000668.1:g.87725533A>G GRCh37
NC_000006.10:g.87782252A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305344.7:c.481A>G MANE Select ENSP00000307766.4:p.Arg161Gly
ENST00000305344.6:c.481A>G ENSP00000307766.4:p.Arg161Gly
NM_000865.2:c.481A>G NP_000856.1:p.Arg161Gly
XM_011535789.1:c.481A>G XP_011534091.1:p.Arg161Gly
XM_011535790.1:c.481A>G XP_011534092.1:p.Arg161Gly
XM_011535789.2:c.481A>G XP_011534091.1:p.Arg161Gly
NM_000865.3:c.481A>G MANE Select NP_000856.1:p.Arg161Gly