Canonical Allele Identifier: CA2711609716

Gene: HCRTR2

Linked Data

• dbSNP Id: rs1767076538

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.55276361A>T , CM000668.2:g.55276361A>T	GRCh38
NC_000006.11:g.55141159A>T , CM000668.1:g.55141159A>T	GRCh37
NC_000006.10:g.55249118A>T	NCBI36
NG_012447.1:g.107089A>T
NG_012447.2:g.174902A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370862.4:c.763-1019A>T MANE Select	ENSP00000359899.3:n.763-1019A>T
ENST00000370862.3:c.763-1019A>T	ENSP00000359899.3:n.763-1019A>T
ENST00000615358.4:c.763-1019A>T	ENSP00000477548.1:n.763-1019A>T
NM_001526.3:c.763-1019A>T	NP_001517.2:n.763-1019A>T
XM_011514542.1:c.568-1019A>T	XP_011512844.1:n.568-1019A>T
NM_001526.4:c.763-1019A>T	NP_001517.2:n.763-1019A>T
XM_017010798.1:c.763-1019A>T	XP_016866287.1:n.763-1019A>T
NM_001384272.1:c.763-1019A>T MANE Select	NP_001371201.1:n.763-1019A>T
NM_001526.5:c.763-1019A>T	NP_001517.2:n.763-1019A>T