Canonical Allele Identifier: CA2711611232

Gene: HCRTR2

Linked Data

• dbSNP Id: rs1767232738

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.55283334A>G , CM000668.2:g.55283334A>G	GRCh38
NC_000006.11:g.55148132A>G , CM000668.1:g.55148132A>G	GRCh37
NC_000006.10:g.55256091A>G	NCBI36
NG_012447.1:g.114062A>G
NG_012447.2:g.181875A>G

Transcript Alleles

HGVS	Amino-acid change
XM_017010798.1:c.1331+884A>G	XP_016866287.1:n.1331+884A>G