Canonical Allele Identifier: CA450593415
Gene: HCRTR2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.55113438T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.55248640T>G , CM000668.2:g.55248640T>G GRCh38
NC_000006.11:g.55113438T>G , CM000668.1:g.55113438T>G GRCh37
NC_000006.10:g.55221397T>G NCBI36
NG_012447.1:g.79368T>G
NG_012447.2:g.147181T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000370862.4:c.225T>G MANE Select ENSP00000359899.3:p.Val75=
ENST00000370862.3:c.225T>G ENSP00000359899.3:p.Val75=
ENST00000615358.4:c.225T>G ENSP00000477548.1:p.Val75=
NM_001526.3:c.225T>G NP_001517.2:p.Val75=
XM_011514542.1:c.30T>G XP_011512844.1:p.Val10=
NM_001526.4:c.225T>G NP_001517.2:p.Val75=
XM_017010798.1:c.225T>G XP_016866287.1:p.Val75=
NM_001384272.1:c.225T>G MANE Select NP_001371201.1:p.Val75=
NM_001526.5:c.225T>G NP_001517.2:p.Val75=