Canonical Allele Identifier: CA2711474797

Gene: HCRTR2

Linked Data

• dbSNP Id: rs138345054

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.55283389A>G , CM000668.2:g.55283389A>G	GRCh38
NC_000006.11:g.55148187A>G , CM000668.1:g.55148187A>G	GRCh37
NC_000006.10:g.55256146A>G	NCBI36
NG_012447.1:g.114117A>G
NG_012447.2:g.181930A>G

Transcript Alleles

HGVS	Amino-acid Change
XM_017010798.1:c.1331+939A>G	XP_016866287.1:n.1331+939A>G