Canonical Allele Identifier: CA2711540832

Gene: HCRTR2

Linked Data

• dbSNP Id: rs1562033963

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.55283301T>C , CM000668.2:g.55283301T>C	GRCh38
NC_000006.11:g.55148099T>C , CM000668.1:g.55148099T>C	GRCh37
NC_000006.10:g.55256058T>C	NCBI36
NG_012447.1:g.114029T>C
NG_012447.2:g.181842T>C

Transcript Alleles

HGVS	Amino-acid Change
XM_017010798.1:c.1331+851T>C	XP_016866287.1:n.1331+851T>C