Canonical Allele Identifier: CA365058085
Gene: HTR1E HGNC NCBI

Linked Data

dbSNP Id: rs1337278187
gnomAD v2: 6-87725646-A-G
gnomAD v3: 6-87015928-A-G
gnomAD v4: 6-87015928-A-G
MyVariant Identifiers: chr6:g.87725646A>G (hg19) chr6:g.87015928A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.87015928A>G , CM000668.2:g.87015928A>G GRCh38
NC_000006.11:g.87725646A>G , CM000668.1:g.87725646A>G GRCh37
NC_000006.10:g.87782365A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305344.7:c.594A>G MANE Select ENSP00000307766.4:p.Ile198Met
ENST00000305344.6:c.594A>G ENSP00000307766.4:p.Ile198Met
NM_000865.2:c.594A>G NP_000856.1:p.Ile198Met
XM_011535789.1:c.594A>G XP_011534091.1:p.Ile198Met
XM_011535790.1:c.594A>G XP_011534092.1:p.Ile198Met
XM_011535789.2:c.594A>G XP_011534091.1:p.Ile198Met
NM_000865.3:c.594A>G MANE Select NP_000856.1:p.Ile198Met
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