Canonical Allele Identifier: CA609568648
Gene: HTR2A HGNC NCBI

Linked Data

dbSNP Id: rs1453920702
gnomAD v2: 13-47458099-C-G
gnomAD v3: 13-46883964-C-G
gnomAD v4: 13-46883964-C-G
MyVariant Identifiers: chr13:g.47458099C>G (hg19) chr13:g.46883964C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46883964C>G , CM000675.2:g.46883964C>G GRCh38
NC_000013.10:g.47458099C>G , CM000675.1:g.47458099C>G GRCh37
NC_000013.9:g.46356100C>G NCBI36
NG_013011.1:g.18071G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000542664.4:c.613+8426G>C MANE Select ENSP00000437737.1:n.613+8426G>C
ENST00000543956.5:c.124+8426G>C ENSP00000441861.2:n.124+8426G>C
ENST00000378688.8:c.613+8426G>C ENSP00000367959.3:n.613+8426G>C
ENST00000542664.3:c.613+8426G>C ENSP00000437737.1:n.613+8426G>C
ENST00000543956.4:c.361+8426G>C ENSP00000441861.1:n.361+8426G>C
NM_000621.4:c.613+8426G>C NP_000612.1:n.613+8426G>C
NM_001165947.2:c.361+8426G>C NP_001159419.1:n.361+8426G>C
NM_000621.5:c.613+8426G>C MANE Select NP_000612.1:n.613+8426G>C
NM_001165947.5:c.124+8426G>C NP_001159419.2:n.124+8426G>C
NM_001378924.1:c.613+8426G>C NP_001365853.1:n.613+8426G>C
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