Canonical Allele Identifier: CA2533280730

Gene: HCRTR2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.55269391G>A , CM000668.2:g.55269391G>A	GRCh38
NC_000006.11:g.55134189G>A , CM000668.1:g.55134189G>A	GRCh37
NC_000006.10:g.55242148G>A	NCBI36
NG_012447.1:g.100119G>A
NG_012447.2:g.167932G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000370862.4:c.762+5569G>A MANE Select	ENSP00000359899.3:n.762+5569G>A
ENST00000370862.3:c.762+5569G>A	ENSP00000359899.3:n.762+5569G>A
ENST00000615358.4:c.762+5569G>A	ENSP00000477548.1:n.762+5569G>A
NM_001526.3:c.762+5569G>A	NP_001517.2:n.762+5569G>A
XM_011514542.1:c.567+5569G>A	XP_011512844.1:n.567+5569G>A
NM_001526.4:c.762+5569G>A	NP_001517.2:n.762+5569G>A
XM_017010798.1:c.762+5569G>A	XP_016866287.1:n.762+5569G>A
NM_001384272.1:c.762+5569G>A MANE Select	NP_001371201.1:n.762+5569G>A
NM_001526.5:c.762+5569G>A	NP_001517.2:n.762+5569G>A