Canonical Allele Identifier: CA364609032

Gene: HCRTR2

Linked Data

• MyVariant Identifiers: chr6:g.55113443T>C (hg19) ; chr6:g.55248645T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.55248645T>C , CM000668.2:g.55248645T>C	GRCh38
NC_000006.11:g.55113443T>C , CM000668.1:g.55113443T>C	GRCh37
NC_000006.10:g.55221402T>C	NCBI36
NG_012447.1:g.79373T>C
NG_012447.2:g.147186T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000370862.4:c.230T>C MANE Select	ENSP00000359899.3:p.Val77Ala
ENST00000370862.3:c.230T>C	ENSP00000359899.3:p.Val77Ala
ENST00000615358.4:c.230T>C	ENSP00000477548.1:p.Val77Ala
NM_001526.3:c.230T>C	NP_001517.2:p.Val77Ala
XM_011514542.1:c.35T>C	XP_011512844.1:p.Val12Ala
NM_001526.4:c.230T>C	NP_001517.2:p.Val77Ala
XM_017010798.1:c.230T>C	XP_016866287.1:p.Val77Ala
NM_001384272.1:c.230T>C MANE Select	NP_001371201.1:p.Val77Ala
NM_001526.5:c.230T>C	NP_001517.2:p.Val77Ala