Canonical Allele Identifier: CA388154786
Gene: HTR2A HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.47469910G>C (hg19) chr13:g.46895775G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46895775G>C , CM000675.2:g.46895775G>C GRCh38
NC_000013.10:g.47469910G>C , CM000675.1:g.47469910G>C GRCh37
NC_000013.9:g.46367911G>C NCBI36
NG_013011.1:g.6260C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000542664.4:c.132C>G MANE Select ENSP00000437737.1:p.Asn44Lys
ENST00000543956.5:c.-78+899C>G ENSP00000441861.2:n.-78+899C>G
ENST00000378688.8:c.132C>G ENSP00000367959.3:p.Asn44Lys
ENST00000542664.3:c.132C>G ENSP00000437737.1:p.Asn44Lys
ENST00000543956.4:c.160+899C>G ENSP00000441861.1:n.160+899C>G
ENST00000612998.1:c.39C>G ENSP00000482708.1:p.Asn13Lys
NM_000621.4:c.132C>G NP_000612.1:p.Asn44Lys
NM_001165947.2:c.160+899C>G NP_001159419.1:n.160+899C>G
NM_000621.5:c.132C>G MANE Select NP_000612.1:p.Asn44Lys
NM_001165947.5:c.-78+899C>G NP_001159419.2:n.-78+899C>G
NM_001378924.1:c.132C>G NP_001365853.1:p.Asn44Lys
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