Canonical Allele Identifier: CA139611700

Gene: HCRTR2

Linked Data

• dbSNP Id: rs1057485629
• MyVariant Identifiers: chr6:g.55148061G>T (hg19) ; chr6:g.55283263G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.55283263G>T , CM000668.2:g.55283263G>T	GRCh38
NC_000006.11:g.55148061G>T , CM000668.1:g.55148061G>T	GRCh37
NC_000006.10:g.55256020G>T	NCBI36
NG_012447.1:g.113991G>T
NG_012447.2:g.181804G>T

Transcript Alleles

HGVS	Amino-acid Change
XM_017010798.1:c.1331+813G>T	XP_016866287.1:n.1331+813G>T