Canonical Allele Identifier: CA451355078
Gene: HTR1E HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.87725622G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.87015904G>C , CM000668.2:g.87015904G>C GRCh38
NC_000006.11:g.87725622G>C , CM000668.1:g.87725622G>C GRCh37
NC_000006.10:g.87782341G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305344.7:c.570G>C MANE Select ENSP00000307766.4:p.Ala190=
ENST00000305344.6:c.570G>C ENSP00000307766.4:p.Ala190=
NM_000865.2:c.570G>C NP_000856.1:p.Ala190=
XM_011535789.1:c.570G>C XP_011534091.1:p.Ala190=
XM_011535790.1:c.570G>C XP_011534092.1:p.Ala190=
XM_011535789.2:c.570G>C XP_011534091.1:p.Ala190=
NM_000865.3:c.570G>C MANE Select NP_000856.1:p.Ala190=
Search 100 bp 5'
Search 100 bp 3'