Canonical Allele Identifier: CA2771135087
Gene: HCRTR2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.55269472T>A , CM000668.2:g.55269472T>A GRCh38
NC_000006.11:g.55134270T>A , CM000668.1:g.55134270T>A GRCh37
NC_000006.10:g.55242229T>A NCBI36
NG_012447.1:g.100200T>A
NG_012447.2:g.168013T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000370862.4:c.762+5650T>A MANE Select ENSP00000359899.3:n.762+5650T>A
ENST00000370862.3:c.762+5650T>A ENSP00000359899.3:n.762+5650T>A
ENST00000615358.4:c.762+5650T>A ENSP00000477548.1:n.762+5650T>A
NM_001526.3:c.762+5650T>A NP_001517.2:n.762+5650T>A
XM_011514542.1:c.567+5650T>A XP_011512844.1:n.567+5650T>A
NM_001526.4:c.762+5650T>A NP_001517.2:n.762+5650T>A
XM_017010798.1:c.762+5650T>A XP_016866287.1:n.762+5650T>A
NM_001384272.1:c.762+5650T>A MANE Select NP_001371201.1:n.762+5650T>A
NM_001526.5:c.762+5650T>A NP_001517.2:n.762+5650T>A
Search 100 bp 5'
Search 100 bp 3'