Canonical Allele Identifier: CA826027459

Gene: HCRTR2

Linked Data

• dbSNP Id: rs1172029470
• gnomAD v3: 6-55269290-T-A
• gnomAD v4: 6-55269290-T-A
• MyVariant Identifiers: chr6:g.55134088T>A (hg19) ; chr6:g.55269290T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.55269290T>A , CM000668.2:g.55269290T>A	GRCh38
NC_000006.11:g.55134088T>A , CM000668.1:g.55134088T>A	GRCh37
NC_000006.10:g.55242047T>A	NCBI36
NG_012447.1:g.100018T>A
NG_012447.2:g.167831T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370862.4:c.762+5468T>A MANE Select	ENSP00000359899.3:n.762+5468T>A
ENST00000370862.3:c.762+5468T>A	ENSP00000359899.3:n.762+5468T>A
ENST00000615358.4:c.762+5468T>A	ENSP00000477548.1:n.762+5468T>A
NM_001526.3:c.762+5468T>A	NP_001517.2:n.762+5468T>A
XM_011514542.1:c.567+5468T>A	XP_011512844.1:n.567+5468T>A
NM_001526.4:c.762+5468T>A	NP_001517.2:n.762+5468T>A
XM_017010798.1:c.762+5468T>A	XP_016866287.1:n.762+5468T>A
NM_001384272.1:c.762+5468T>A MANE Select	NP_001371201.1:n.762+5468T>A
NM_001526.5:c.762+5468T>A	NP_001517.2:n.762+5468T>A