Canonical Allele Identifier: CA365058163
Gene: HTR1E HGNC NCBI

Linked Data

dbSNP Id: rs2127834932
gnomAD v3: 6-87015965-A-G
gnomAD v4: 6-87015965-A-G
MyVariant Identifiers: chr6:g.87725683A>G (hg19) chr6:g.87015965A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.87015965A>G , CM000668.2:g.87015965A>G GRCh38
NC_000006.11:g.87725683A>G , CM000668.1:g.87725683A>G GRCh37
NC_000006.10:g.87782402A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305344.7:c.631A>G MANE Select ENSP00000307766.4:p.Ser211Gly
ENST00000305344.6:c.631A>G ENSP00000307766.4:p.Ser211Gly
NM_000865.2:c.631A>G NP_000856.1:p.Ser211Gly
XM_011535789.1:c.631A>G XP_011534091.1:p.Ser211Gly
XM_011535790.1:c.631A>G XP_011534092.1:p.Ser211Gly
XM_011535789.2:c.631A>G XP_011534091.1:p.Ser211Gly
NM_000865.3:c.631A>G MANE Select NP_000856.1:p.Ser211Gly
Search 100 bp 5'
Search 100 bp 3'