Canonical Allele Identifier: CA249254257
Gene: HTR2A HGNC NCBI

Linked Data

dbSNP Id: rs760783225
MyVariant Identifiers: chr13:g.47458090_47458091insG (hg19) chr13:g.46883955_46883956insG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46883959dup , CM000675.2:g.46883959dup GRCh38
NC_000013.10:g.47458094dup , CM000675.1:g.47458094dup GRCh37
NC_000013.9:g.46356095dup NCBI36
NG_013011.1:g.18079dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000542664.4:c.613+8434dup MANE Select ENSP00000437737.1:n.613+8434dup
ENST00000543956.5:c.124+8434dup ENSP00000441861.2:n.124+8434dup
ENST00000378688.8:c.613+8434dup ENSP00000367959.3:n.613+8434dup
ENST00000542664.3:c.613+8434dup ENSP00000437737.1:n.613+8434dup
ENST00000543956.4:c.361+8434dup ENSP00000441861.1:n.361+8434dup
NM_000621.4:c.613+8434dup NP_000612.1:n.613+8434dup
NM_001165947.2:c.361+8434dup NP_001159419.1:n.361+8434dup
NM_000621.5:c.613+8434dup MANE Select NP_000612.1:n.613+8434dup
NM_001165947.5:c.124+8434dup NP_001159419.2:n.124+8434dup
NM_001378924.1:c.613+8434dup NP_001365853.1:n.613+8434dup
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