Canonical Allele Identifier: CA3863432

Gene: HCRTR2

Linked Data

• dbSNP Id: rs768299252
• ExAC: 6:55113441 T / C
• gnomAD v2: 6-55113441-T-C
• gnomAD v4: 6-55248643-T-C
• MyVariant Identifiers: chr6:g.55113441T>C (hg19) ; chr6:g.55248643T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.55248643T>C , CM000668.2:g.55248643T>C	GRCh38
NC_000006.11:g.55113441T>C , CM000668.1:g.55113441T>C	GRCh37
NC_000006.10:g.55221400T>C	NCBI36
NG_012447.1:g.79371T>C
NG_012447.2:g.147184T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000370862.4:c.228T>C MANE Select	ENSP00000359899.3:p.Cys76=
ENST00000370862.3:c.228T>C	ENSP00000359899.3:p.Cys76=
ENST00000615358.4:c.228T>C	ENSP00000477548.1:p.Cys76=
NM_001526.3:c.228T>C	NP_001517.2:p.Cys76=
XM_011514542.1:c.33T>C	XP_011512844.1:p.Cys11=
NM_001526.4:c.228T>C	NP_001517.2:p.Cys76=
XM_017010798.1:c.228T>C	XP_016866287.1:p.Cys76=
NM_001384272.1:c.228T>C MANE Select	NP_001371201.1:p.Cys76=
NM_001526.5:c.228T>C	NP_001517.2:p.Cys76=