Canonical Allele Identifier: CA917753334
Gene: HCRTR2 HGNC NCBI

Linked Data

dbSNP Id: rs1562021448
gnomAD v4: 6-55248625-TC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.55248626del , CM000668.2:g.55248626del GRCh38
NC_000006.11:g.55113424del , CM000668.1:g.55113424del GRCh37
NC_000006.10:g.55221383del NCBI36
NG_012447.1:g.79354del
NG_012447.2:g.147167del

Transcript Alleles

HGVS Amino-acid change
ENST00000370862.4:c.224-13del MANE Select ENSP00000359899.3:n.224-13del
ENST00000370862.3:c.224-13del ENSP00000359899.3:n.224-13del
ENST00000615358.4:c.224-13del ENSP00000477548.1:n.224-13del
NM_001526.3:c.224-13del NP_001517.2:n.224-13del
XM_011514542.1:c.29-13del XP_011512844.1:n.29-13del
NM_001526.4:c.224-13del NP_001517.2:n.224-13del
XM_017010798.1:c.224-13del XP_016866287.1:n.224-13del
NM_001384272.1:c.224-13del MANE Select NP_001371201.1:n.224-13del
NM_001526.5:c.224-13del NP_001517.2:n.224-13del
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