Canonical Allele Identifier: CA567490901

Gene: HCRTR2

Linked Data

• dbSNP Id: rs1168666932
• gnomAD v2: 6-55147995-A-G
• gnomAD v3: 6-55283197-A-G
• gnomAD v4: 6-55283197-A-G
• MyVariant Identifiers: chr6:g.55147995A>G (hg19) ; chr6:g.55283197A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.55283197A>G , CM000668.2:g.55283197A>G	GRCh38
NC_000006.11:g.55147995A>G , CM000668.1:g.55147995A>G	GRCh37
NC_000006.10:g.55255954A>G	NCBI36
NG_012447.1:g.113925A>G
NG_012447.2:g.181738A>G

Transcript Alleles

HGVS	Amino-acid Change
XM_017010798.1:c.1331+747A>G	XP_016866287.1:n.1331+747A>G