Canonical Allele Identifier: CA3863423
Gene: HCRTR2 HGNC NCBI

Linked Data

dbSNP Id: rs3122169

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.55248613C>A , CM000668.2:g.55248613C>A GRCh38
NC_000006.11:g.55113411C>A , CM000668.1:g.55113411C>A GRCh37
NC_000006.10:g.55221370C>A NCBI36
NG_012447.1:g.79341C>A
NG_012447.2:g.147154C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000370862.3:c.224-26C>A ENSP00000359899.3:p.=
ENST00000615358.4:c.224-26C>A ENSP00000477548.1:p.=
NM_001526.3:c.224-26C>A NP_001517.2:p.=
XM_011514542.1:c.29-26C>A XP_011512844.1:p.=
NM_001526.4:c.224-26C>A NP_001517.2:p.=
XM_017010798.1:c.224-26C>A XP_016866287.1:p.=
NM_001384272.1:c.224-26C>A MANE Select NP_001371201.1:p.=
NM_001526.5:c.224-26C>A NP_001517.2:p.=