Canonical Allele Identifier: CA139611708

Gene: HCRTR2

Linked Data

• dbSNP Id: rs999895432
• MyVariant Identifiers: chr6:g.55148100G>A (hg19) ; chr6:g.55283302G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.55283302G>A , CM000668.2:g.55283302G>A	GRCh38
NC_000006.11:g.55148100G>A , CM000668.1:g.55148100G>A	GRCh37
NC_000006.10:g.55256059G>A	NCBI36
NG_012447.1:g.114030G>A
NG_012447.2:g.181843G>A

Transcript Alleles

HGVS	Amino-acid Change
XM_017010798.1:c.1331+852G>A	XP_016866287.1:n.1331+852G>A