Canonical Allele Identifier: CA1089197960

Gene: HCRTR2

Linked Data

• dbSNP Id: rs1765107595
• gnomAD v3: 6-55180219-T-TACTCAAAAGTTTA
• gnomAD v4: 6-55180219-T-TACTCAAAAGTTTA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.55180220_55180232dup , CM000668.2:g.55180220_55180232dup	GRCh38
NC_000006.11:g.55045018_55045030dup , CM000668.1:g.55045018_55045030dup	GRCh37
NC_000006.10:g.55152977_55152989dup	NCBI36
NG_012447.1:g.10948_10960dup
NG_012447.2:g.78761_78773dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000370862.4:c.223+5410_223+5422dup MANE Select	ENSP00000359899.3:n.223+5410_223+5422dup
ENST00000370862.3:c.223+5410_223+5422dup	ENSP00000359899.3:n.223+5410_223+5422dup
ENST00000615358.4:c.223+5410_223+5422dup	ENSP00000477548.1:n.223+5410_223+5422dup
NM_001526.3:c.223+5410_223+5422dup	NP_001517.2:n.223+5410_223+5422dup
NM_001526.4:c.223+5410_223+5422dup	NP_001517.2:n.223+5410_223+5422dup
XM_017010798.1:c.223+5410_223+5422dup	XP_016866287.1:n.223+5410_223+5422dup
NM_001384272.1:c.223+5410_223+5422dup MANE Select	NP_001371201.1:n.223+5410_223+5422dup
NM_001526.5:c.223+5410_223+5422dup	NP_001517.2:n.223+5410_223+5422dup