Canonical Allele Identifier: CA139611714

Gene: HCRTR2

Linked Data

• dbSNP Id: rs955391525
• MyVariant Identifiers: chr6:g.55148118G>T (hg19) ; chr6:g.55283320G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.55283320G>T , CM000668.2:g.55283320G>T	GRCh38
NC_000006.11:g.55148118G>T , CM000668.1:g.55148118G>T	GRCh37
NC_000006.10:g.55256077G>T	NCBI36
NG_012447.1:g.114048G>T
NG_012447.2:g.181861G>T

Transcript Alleles

HGVS	Amino-acid Change
XM_017010798.1:c.1331+870G>T	XP_016866287.1:n.1331+870G>T