Canonical Allele Identifier: CA2711495538

Gene: HCRTR2

Linked Data

• dbSNP Id: rs999463766

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.55283317A>C , CM000668.2:g.55283317A>C	GRCh38
NC_000006.11:g.55148115A>C , CM000668.1:g.55148115A>C	GRCh37
NC_000006.10:g.55256074A>C	NCBI36
NG_012447.1:g.114045A>C
NG_012447.2:g.181858A>C

Transcript Alleles

HGVS	Amino-acid Change
XM_017010798.1:c.1331+867A>C	XP_016866287.1:n.1331+867A>C