Canonical Allele Identifier: CA388151017
Gene: HTR2A HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.47409197A>C (hg19) chr13:g.46835062A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46835062A>C , CM000675.2:g.46835062A>C GRCh38
NC_000013.10:g.47409197A>C , CM000675.1:g.47409197A>C GRCh37
NC_000013.9:g.46307198A>C NCBI36
NG_013011.1:g.66973T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000542664.4:c.1191T>G MANE Select ENSP00000437737.1:p.Cys397Trp
ENST00000543956.5:c.702T>G ENSP00000441861.2:p.Cys234Trp
ENST00000378688.8:c.1191T>G ENSP00000367959.3:p.Cys397Trp
ENST00000542664.3:c.1191T>G ENSP00000437737.1:p.Cys397Trp
ENST00000543956.4:c.939T>G ENSP00000441861.1:p.Cys313Trp
NM_000621.4:c.1191T>G NP_000612.1:p.Cys397Trp
NM_001165947.2:c.939T>G NP_001159419.1:p.Cys313Trp
NM_000621.5:c.1191T>G MANE Select NP_000612.1:p.Cys397Trp
NM_001165947.5:c.702T>G NP_001159419.2:p.Cys234Trp
NM_001378924.1:c.1191T>G NP_001365853.1:p.Cys397Trp
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