Canonical Allele Identifier: CA1089240347

Gene: HCRTR2

Linked Data

• dbSNP Id: rs1767075355
• gnomAD v3: 6-55276294-T-C
• gnomAD v4: 6-55276294-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.55276294T>C , CM000668.2:g.55276294T>C	GRCh38
NC_000006.11:g.55141092T>C , CM000668.1:g.55141092T>C	GRCh37
NC_000006.10:g.55249051T>C	NCBI36
NG_012447.1:g.107022T>C
NG_012447.2:g.174835T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000370862.4:c.763-1086T>C MANE Select	ENSP00000359899.3:n.763-1086T>C
ENST00000370862.3:c.763-1086T>C	ENSP00000359899.3:n.763-1086T>C
ENST00000615358.4:c.763-1086T>C	ENSP00000477548.1:n.763-1086T>C
NM_001526.3:c.763-1086T>C	NP_001517.2:n.763-1086T>C
XM_011514542.1:c.568-1086T>C	XP_011512844.1:n.568-1086T>C
NM_001526.4:c.763-1086T>C	NP_001517.2:n.763-1086T>C
XM_017010798.1:c.763-1086T>C	XP_016866287.1:n.763-1086T>C
NM_001384272.1:c.763-1086T>C MANE Select	NP_001371201.1:n.763-1086T>C
NM_001526.5:c.763-1086T>C	NP_001517.2:n.763-1086T>C