Canonical Allele Identifier: CA826027492

Gene: HCRTR2

Linked Data

• dbSNP Id: rs1464033205
• gnomAD v3: 6-55269392-A-G
• gnomAD v4: 6-55269392-A-G
• MyVariant Identifiers: chr6:g.55134190A>G (hg19) ; chr6:g.55269392A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.55269392A>G , CM000668.2:g.55269392A>G	GRCh38
NC_000006.11:g.55134190A>G , CM000668.1:g.55134190A>G	GRCh37
NC_000006.10:g.55242149A>G	NCBI36
NG_012447.1:g.100120A>G
NG_012447.2:g.167933A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000370862.4:c.762+5570A>G MANE Select	ENSP00000359899.3:n.762+5570A>G
ENST00000370862.3:c.762+5570A>G	ENSP00000359899.3:n.762+5570A>G
ENST00000615358.4:c.762+5570A>G	ENSP00000477548.1:n.762+5570A>G
NM_001526.3:c.762+5570A>G	NP_001517.2:n.762+5570A>G
XM_011514542.1:c.567+5570A>G	XP_011512844.1:n.567+5570A>G
NM_001526.4:c.762+5570A>G	NP_001517.2:n.762+5570A>G
XM_017010798.1:c.762+5570A>G	XP_016866287.1:n.762+5570A>G
NM_001384272.1:c.762+5570A>G MANE Select	NP_001371201.1:n.762+5570A>G
NM_001526.5:c.762+5570A>G	NP_001517.2:n.762+5570A>G