Canonical Allele Identifier: CA364609018
Gene: HCRTR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.55248639T>C , CM000668.2:g.55248639T>C GRCh38
NC_000006.11:g.55113437T>C , CM000668.1:g.55113437T>C GRCh37
NC_000006.10:g.55221396T>C NCBI36
NG_012447.1:g.79367T>C
NG_012447.2:g.147180T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000370862.4:c.224T>C MANE Select ENSP00000359899.3:p.Val75Ala
ENST00000370862.3:c.224T>C ENSP00000359899.3:p.Val75Ala
ENST00000615358.4:c.224T>C ENSP00000477548.1:p.Val75Ala
NM_001526.3:c.224T>C NP_001517.2:p.Val75Ala
XM_011514542.1:c.29T>C XP_011512844.1:p.Val10Ala
NM_001526.4:c.224T>C NP_001517.2:p.Val75Ala
XM_017010798.1:c.224T>C XP_016866287.1:p.Val75Ala
NM_001384272.1:c.224T>C MANE Select NP_001371201.1:p.Val75Ala
NM_001526.5:c.224T>C NP_001517.2:p.Val75Ala