Canonical Allele Identifier: CA2711608097

Gene: HCRTR2

Linked Data

• dbSNP Id: rs1766926640

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.55269332T>C , CM000668.2:g.55269332T>C	GRCh38
NC_000006.11:g.55134130T>C , CM000668.1:g.55134130T>C	GRCh37
NC_000006.10:g.55242089T>C	NCBI36
NG_012447.1:g.100060T>C
NG_012447.2:g.167873T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370862.4:c.762+5510T>C MANE Select	ENSP00000359899.3:n.762+5510T>C
ENST00000370862.3:c.762+5510T>C	ENSP00000359899.3:n.762+5510T>C
ENST00000615358.4:c.762+5510T>C	ENSP00000477548.1:n.762+5510T>C
NM_001526.3:c.762+5510T>C	NP_001517.2:n.762+5510T>C
XM_011514542.1:c.567+5510T>C	XP_011512844.1:n.567+5510T>C
NM_001526.4:c.762+5510T>C	NP_001517.2:n.762+5510T>C
XM_017010798.1:c.762+5510T>C	XP_016866287.1:n.762+5510T>C
NM_001384272.1:c.762+5510T>C MANE Select	NP_001371201.1:n.762+5510T>C
NM_001526.5:c.762+5510T>C	NP_001517.2:n.762+5510T>C