Canonical Allele Identifier: CA826030903

Gene: HCRTR2

Linked Data

• dbSNP Id: rs1266631880
• gnomAD v3: 6-55276364-C-T
• gnomAD v4: 6-55276364-C-T
• MyVariant Identifiers: chr6:g.55141162C>T (hg19) ; chr6:g.55276364C>T (hg38)

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