Canonical Allele Identifier: CA826030903
Gene: HCRTR2 HGNC NCBI

Linked Data

dbSNP Id: rs1266631880
gnomAD v3: 6-55276364-C-T
gnomAD v4: 6-55276364-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.55276364C>T , CM000668.2:g.55276364C>T GRCh38
NC_000006.11:g.55141162C>T , CM000668.1:g.55141162C>T GRCh37
NC_000006.10:g.55249121C>T NCBI36
NG_012447.1:g.107092C>T
NG_012447.2:g.174905C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000370862.4:c.763-1016C>T MANE Select ENSP00000359899.3:n.763-1016C>T
ENST00000370862.3:c.763-1016C>T ENSP00000359899.3:n.763-1016C>T
ENST00000615358.4:c.763-1016C>T ENSP00000477548.1:n.763-1016C>T
NM_001526.3:c.763-1016C>T NP_001517.2:n.763-1016C>T
XM_011514542.1:c.568-1016C>T XP_011512844.1:n.568-1016C>T
NM_001526.4:c.763-1016C>T NP_001517.2:n.763-1016C>T
XM_017010798.1:c.763-1016C>T XP_016866287.1:n.763-1016C>T
NM_001384272.1:c.763-1016C>T MANE Select NP_001371201.1:n.763-1016C>T
NM_001526.5:c.763-1016C>T NP_001517.2:n.763-1016C>T