Canonical Allele Identifier: CA364609027

Gene: HCRTR2

Linked Data

• MyVariant Identifiers: chr6:g.55113441T>G (hg19) ; chr6:g.55248643T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.55248643T>G , CM000668.2:g.55248643T>G	GRCh38
NC_000006.11:g.55113441T>G , CM000668.1:g.55113441T>G	GRCh37
NC_000006.10:g.55221400T>G	NCBI36
NG_012447.1:g.79371T>G
NG_012447.2:g.147184T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370862.4:c.228T>G MANE Select	ENSP00000359899.3:p.Cys76Trp
ENST00000370862.3:c.228T>G	ENSP00000359899.3:p.Cys76Trp
ENST00000615358.4:c.228T>G	ENSP00000477548.1:p.Cys76Trp
NM_001526.3:c.228T>G	NP_001517.2:p.Cys76Trp
XM_011514542.1:c.33T>G	XP_011512844.1:p.Cys11Trp
NM_001526.4:c.228T>G	NP_001517.2:p.Cys76Trp
XM_017010798.1:c.228T>G	XP_016866287.1:p.Cys76Trp
NM_001384272.1:c.228T>G MANE Select	NP_001371201.1:p.Cys76Trp
NM_001526.5:c.228T>G	NP_001517.2:p.Cys76Trp