Canonical Allele Identifier: CA2711608090
Gene: HCRTR2 HGNC NCBI

Linked Data

dbSNP Id: rs1766926274
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.55269320G>A , CM000668.2:g.55269320G>A GRCh38
NC_000006.11:g.55134118G>A , CM000668.1:g.55134118G>A GRCh37
NC_000006.10:g.55242077G>A NCBI36
NG_012447.1:g.100048G>A
NG_012447.2:g.167861G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000370862.4:c.762+5498G>A MANE Select ENSP00000359899.3:n.762+5498G>A
ENST00000370862.3:c.762+5498G>A ENSP00000359899.3:n.762+5498G>A
ENST00000615358.4:c.762+5498G>A ENSP00000477548.1:n.762+5498G>A
NM_001526.3:c.762+5498G>A NP_001517.2:n.762+5498G>A
XM_011514542.1:c.567+5498G>A XP_011512844.1:n.567+5498G>A
NM_001526.4:c.762+5498G>A NP_001517.2:n.762+5498G>A
XM_017010798.1:c.762+5498G>A XP_016866287.1:n.762+5498G>A
NM_001384272.1:c.762+5498G>A MANE Select NP_001371201.1:n.762+5498G>A
NM_001526.5:c.762+5498G>A NP_001517.2:n.762+5498G>A
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