Canonical Allele Identifier: CA567488246

Gene: HCRTR2

Linked Data

• dbSNP Id: rs1298180542
• gnomAD v2: 6-55141145-AAAG-A
• gnomAD v3: 6-55276347-AAAG-A
• gnomAD v4: 6-55276347-AAAG-A
• MyVariant Identifiers: chr6:g.55141146_55141148del (hg19) ; chr6:g.55276348_55276350del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.55276349_55276351del , CM000668.2:g.55276349_55276351del	GRCh38
NC_000006.11:g.55141147_55141149del , CM000668.1:g.55141147_55141149del	GRCh37
NC_000006.10:g.55249106_55249108del	NCBI36
NG_012447.1:g.107077_107079del
NG_012447.2:g.174890_174892del

Transcript Alleles

HGVS	Amino-acid change
ENST00000370862.4:c.763-1031_763-1029del MANE Select	ENSP00000359899.3:n.763-1031_763-1029del
ENST00000370862.3:c.763-1031_763-1029del	ENSP00000359899.3:n.763-1031_763-1029del
ENST00000615358.4:c.763-1031_763-1029del	ENSP00000477548.1:n.763-1031_763-1029del
NM_001526.3:c.763-1031_763-1029del	NP_001517.2:n.763-1031_763-1029del
XM_011514542.1:c.568-1031_568-1029del	XP_011512844.1:n.568-1031_568-1029del
NM_001526.4:c.763-1031_763-1029del	NP_001517.2:n.763-1031_763-1029del
XM_017010798.1:c.763-1031_763-1029del	XP_016866287.1:n.763-1031_763-1029del
NM_001384272.1:c.763-1031_763-1029del MANE Select	NP_001371201.1:n.763-1031_763-1029del
NM_001526.5:c.763-1031_763-1029del	NP_001517.2:n.763-1031_763-1029del