Canonical Allele Identifier: CA3913258
Gene: HTR1E HGNC NCBI

Linked Data

dbSNP Id: rs750676240
ExAC: 6:87725521 C / G
gnomAD v2: 6-87725521-C-G
gnomAD v4: 6-87015803-C-G
MyVariant Identifiers: chr6:g.87725521C>G (hg19) chr6:g.87015803C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.87015803C>G , CM000668.2:g.87015803C>G GRCh38
NC_000006.11:g.87725521C>G , CM000668.1:g.87725521C>G GRCh37
NC_000006.10:g.87782240C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305344.7:c.469C>G MANE Select ENSP00000307766.4:p.Pro157Ala
ENST00000305344.6:c.469C>G ENSP00000307766.4:p.Pro157Ala
NM_000865.2:c.469C>G NP_000856.1:p.Pro157Ala
XM_011535789.1:c.469C>G XP_011534091.1:p.Pro157Ala
XM_011535790.1:c.469C>G XP_011534092.1:p.Pro157Ala
XM_011535789.2:c.469C>G XP_011534091.1:p.Pro157Ala
NM_000865.3:c.469C>G MANE Select NP_000856.1:p.Pro157Ala
Search 100 bp 5'
Search 100 bp 3'