Canonical Allele Identifier: CA2711585880
Gene: HCRTR2 HGNC NCBI

Linked Data

dbSNP Id: rs1765108754
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.55180262C>A , CM000668.2:g.55180262C>A GRCh38
NC_000006.11:g.55045060C>A , CM000668.1:g.55045060C>A GRCh37
NC_000006.10:g.55153019C>A NCBI36
NG_012447.1:g.10990C>A
NG_012447.2:g.78803C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000370862.4:c.223+5452C>A MANE Select ENSP00000359899.3:n.223+5452C>A
ENST00000370862.3:c.223+5452C>A ENSP00000359899.3:n.223+5452C>A
ENST00000615358.4:c.223+5452C>A ENSP00000477548.1:n.223+5452C>A
NM_001526.3:c.223+5452C>A NP_001517.2:n.223+5452C>A
NM_001526.4:c.223+5452C>A NP_001517.2:n.223+5452C>A
XM_017010798.1:c.223+5452C>A XP_016866287.1:n.223+5452C>A
NM_001384272.1:c.223+5452C>A MANE Select NP_001371201.1:n.223+5452C>A
NM_001526.5:c.223+5452C>A NP_001517.2:n.223+5452C>A
Search 100 bp 5'
Search 100 bp 3'