Canonical Allele Identifier: CA567639511

Gene: HCRTR2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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