Canonical Allele Identifier: CA2497153656
Gene: HCRTR2 HGNC NCBI

Linked Data

dbSNP Id: rs1765109962
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.55180320del , CM000668.2:g.55180320del GRCh38
NC_000006.11:g.55045118del , CM000668.1:g.55045118del GRCh37
NC_000006.10:g.55153077del NCBI36
NG_012447.1:g.11048del
NG_012447.2:g.78861del

Transcript Alleles

HGVS Amino-acid change
ENST00000370862.4:c.223+5510del MANE Select ENSP00000359899.3:n.223+5510del
ENST00000370862.3:c.223+5510del ENSP00000359899.3:n.223+5510del
ENST00000615358.4:c.223+5510del ENSP00000477548.1:n.223+5510del
NM_001526.3:c.223+5510del NP_001517.2:n.223+5510del
NM_001526.4:c.223+5510del NP_001517.2:n.223+5510del
XM_017010798.1:c.223+5510del XP_016866287.1:n.223+5510del
NM_001384272.1:c.223+5510del MANE Select NP_001371201.1:n.223+5510del
NM_001526.5:c.223+5510del NP_001517.2:n.223+5510del
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